Operation Manual M503E027A

Manual No.
: M503-E027
Revision
:A
MOBILE X-RAY SYSTEM
MobileArt Evolution
High Power Type (32 kW)
OPERATION MANUAL
Read this manual carefully to ensure appropriate use,

and keep it with the unit.
About the symbols appearing in this operation

manual
Throughout the text in this manual, warnings and other information essential when using this unit, such as
cautionary or prohibited items, appear classified as per the following:
Mark
Description
States a direct danger that may cause death or serious injury if it is not avoided.
States an indirect or potential danger that may cause death or serious injury if it is not
avoided.
States a danger that may cause slight or medium injury or may cause damage in
equipment or fire if it is not avoided.
States information which helps to use the system correctly.
Provides useful information about operation of this system. Please read the
description when required.
^ Reference
Provides reference information.
Revision History
Revision
Date
First Edition
Apr. 2009
Changes
Added "CXDI-55G/55C and 60C", "8.9 Manufacturer Information", "9 FPD

Upgrade", "9.5.3 Second FPD Kit", "9.5.4 FPD Bag".
Nov. 2009
Correct "2.4 X-Ray Control Panel", "3.3 Moving the System", "3.6 X-Ray
Radiography", "4.1 User Settings", "4.3 Changing Anatomical Program
Parameters", "8.1 Environmental Conditions of EMC (Electro-Magnetic
Compatibility)", "8.2 Specifications", "8.3 Dimensional Drawings", "8.6
Anatomical Program", "8.7 Labels", "8.8 Statement of Compliance [For
Europe]", "9.1 Overview of FPD Upgrade", "9.2 Part Names and
Descriptions", "9.3 Basic Operation", "9.5 Optional Features".
Preface
Thank you for purchasing Shimadzu's mobile X-ray system, the MobileArt Evolution High
Power Type (32 kW) (herein referred to as "the system"). This Operation Manual is
designed to explain the correct operation of this system. Be sure that you have fully read
and understood this Operation Manual prior to using the system.
Be sure only to use this system after you have fully read and understood all warnings,
cautions, and notes contained in this Operation Manual.
This manual does not cover the X-ray tube unit. Read the following manual for the X-ray
tube unit and Heating & Cooling Curve:
X-ray Tube Unit Model Name
X-ray Tube Unit

Document Number
0.7/1.3U163C-36
M535-E318
Be sure to keep this manual nearby for future reference.
Notice
All copyrights regarding this material are property of Shimadzu Corporation.
All or part of these contents shall not be reproduced or duplicated without the express
permission of Shimadzu Corporation.
Content of this manual may be changed or improved without warning.
Although every possible effort has been made to avoid errors while creating this manual,
immediate revision may not be possible in the event that errors or missing information are
detected.
Screen images and illustrations contained in this manual may differ from those in actual
use and are intended for example purposes only. Illustrations may also use partial images.
Copyright
Mobile Art and Mobile DaRt are registered trademarks of Shimadzu Corporation.
This manual does not use the TM or the symbol.
2009 Shimadzu Corporation. All rights reserved.
Preface
Operating Precautions
"Operating Precautions (for Both Safety and the Prevention of

Danger) in the Use of Electric Medical Equipment"
1.
Only an experienced technician should operate the equipment.
2.
When installing the equipment, pay attention to the following items:

(1) Do not install it near water faucet or similar equipment.
(2) Install it away from potential sources of problems such as abnormal
pressure, temperature or humidity, drafts, direct sunlight, dust, chlorine or
sulphur gas.
(3) During transportation and operation of the equipment, avoid tilting,
vibration and sharp impact against it.
(4) Keep the equipment away from areas where chemicals or gases are
stored.
(5) Use only the correct electrical power source with matching frequency,
voltage and current (or wattage).
(6) Check the conditions of the battery power source (power and polarity)
before operating the equipment.
(7) Properly ground the equipment.
3.
Before operating the equipment, pay attention to the following items:

(1) Check the conditions of switch contacts, polarity, dial settings, and
meters, and make sure the equipment performs correctly.
(2) Confirm that the ground is connected properly.
(3) Check all wiring for proper and correct connections.
(4) Pay attention when using more than one unit at a time, because it may
lead to an incorrect diagnosis and cause danger.
(5) Check the condition of the external electric circuit, which will be directly
connected to a patient.
(6) Check the condition of the battery power source.
ii
MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL
M503-E027
Preface
1
4.
While operating the equipment, pay attention to the following items:
(1) Do not exceed time or the amount of equipment use needed for diagnosis
or therapy.
(2) Observe the equipment and patient continuously for early detection of
problems.
(3) When a problem is detected with the equipment or patient, take proper
action to stop the equipment without harming the patient.
(4) Do not let the equipment touch the patient.
5.
After operating the equipment, pay attention to the following items:

(1) Turn off the switches and return the dial to their original positions before
use in the prescribed order. Then, turn off the main power switch.
(2) Do not pull the power cable forcibly from the outlet.
(3) When storing the equipment, pay attention to the following items:
(i)
Keep it away from water.
(ii)
Store it away from potential causes of problems such as abnormal

pressure, temperature and humidity, draft, direct sunlight, dust,
chlorine or sulphur gas.
(iii) During transportation and storage of the equipment, avoid tilting,

vibration and sharp impact against it.
(iv) Store the equipment away from areas where chemicals and gases are
stored.
(4) Clean all attachments, cables and contacts, and store them in one place.
(5) Keep the equipment clean to avoid problems during the next use.
6.
When the equipment is found to be out of order, do not try to repair it.
Display an appropriate sign to indicate that the equipment is out of order,
and contact a Shimadzu service representative for repair.
7.
Do not modify any part of the equipment.
8.
Preventive maintenance
1
1
(1) The equipment and its parts should be periodically checked.

(2) If the equipment has not been in operation for an extended period of time,
test it prior to actual operation to make sure it works correctly and safely.
9.
Concerning other items, operate properly according to the operation

manual.
1
1
M503-E027
iii
Preface
Precautions in Use
When using this equipment, please observe the following precautions for the safety of the operator
and patient.
The responsibility for management of use and maintenance of medical

equipment lies in a user.
This device is restricted to use by, or under supervision of, a diagnostic
radiology technician or a person with a certificate indicating equal proficiency.
Repair and inspection of the inside of the equipment is dangerous. Make sure
to contact our service agency for repair and inspection.
NEVER MODIFY THE EQUIPMENT!

In general, modifications are strictly prohibited by the Regulatory
requirements of the law of the country where device is installed.
Please contact our service agency if it is necessary to modify the device.
PERFORM PERIODIC INSPECTION!

Preventive maintenance is required to maintain long-term safety and
performance of this system.
This manual gives detailed description of occasional and periodic
maintenance and inspection that a user should perform.
As to the maintenance and inspection that specially trained specialists
exclusively can perform, utilize the maintenance agreement offered by our
company.
iv
M503-E027
Preface
1
1
Repair and maintenance of equipment can only be performed by

engineers to whom Shimadzu assigns.
Maintenance must be assigned to specially trained experts. Contact the
Shimadzu Service Representative for repair and maintenance.
1
1
If the operator has no experience in operating the equipment, be sure

that he or she receives instruction on how to operate it from our
engineers or someone who has enough experience to use the
equipment.
In order to operate the equipment safely, an explanation of the operation

needs to be lectured. When installing the equipment, our engineers explain
the operating procedure using this operation manual. Follow their directions
and operate the equipment correctly.
^ Reference "1.5 Operator Profile" P.1-7
1
1
Be sure to Read the Safety Items to Prevent from Explosion or

Electric Shock
1
1
Do NOT use the system in an atmosphere containing combustible gas.

The system is not an AP device. Its use in an atmosphere containing
combustible gas carries the risk of fire or explosion.
1
1
1
M503-E027
Preface
Do NOT use disinfectant sprays that are flammable or could cause an

explosion.
The vapor from a disinfectant spray may ignite, causing life-threatening or
serious injuries and damage to the system.
This equipment has no protection against exposure to liquids. Do NOT

operate this equipment at places with fear of exposure to liquids,
otherwise electric shock may result.
Pay attention so as not to spill liquids on the surface or the inside of this
equipment. In case of liquid spillage on the equipment, stop the operation of
the equipment at once, and contact our service department.
In case when any abnormality is found with the system operation, stop
your operation at once and contact our service agents. Please leave the
whole repair and inspection of the system to them.
Do NOT open the covers and so forth, otherwise electric shock may
result.
Grounding
Connect the power cable plug to a 3-pin grounded socket.
vi
M503-E027
Preface
1
1
Collision and Entanglement

Operator or patient injury can occur if a body part becomes caught between
the arm and the system's main unit. During arm movement, be sure to hold
the specified position and operate the system carefully.
1
1
Charge the battery in a well-ventilated room. Do NOT cover the system

while charging the battery.
1
1
Cautions on Use and Storage
1
Abide by the conditions for correct use and storage.
The locations where this system is used and stored must meet the
following conditions.
Atmosphere:
No explosive or corrosive gases
Using/Storage temperature:
10 to 40 C (only with FPD upgrade: 10 to 35 C)
Relative humidity:
30 to 85% (only with FPD upgrade: 30 to 75%)
(no condensation)
Atmospheric pressure:
700 to 1060 hPa
Note also that there must be no sudden changes in temperature or

humidity.
This causes condensation, which can lead to trouble.
1
1
M503-E027
vii
Preface
Cautions on Cleaning and Disinfection
Be sure to turn OFF the system power before cleaning and disinfecting
the system.
Otherwise, a malfunction may occur in the system, or the system may
operate in an unintended way.
Clean and disinfect the system.

Cleaning and disinfection is very important to ensure that the system can be
used hygienically and safely. You must strictly follow the methods prescribed.
Do NOT apply disinfectant directly, or spray it, onto the system.

If disinfectant gets inside the system, it can cause trouble or accidents.
Do NOT use an organic solvent.

The organic solvent may change the surface in color. If adherent, wipe out
the organic solvent immediately.
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M503-E027
Preface
Cautions Relating to Cellular Telephones
1
1
Do NOT bring cellular telephones or related devices into the

examination room.
Do NOT bring mobile devices that emit electromagnetic waves (e.g. cellular
telephones) into the examination room unless they are switched OFF. Such
devices can exceed the EMC electromagnetic wave standards, and under
some conditions this can impair the proper functioning of the system. In the
worst case, this can cause serious injuries or clinical errors.
1
1
Cautions on the Compatibility of Electromagnetic Fields
1
1
MobileArt Evolution High Power Type (32 kW) needs special

precautions regarding EMC.
The system needs to be installed and use according to the EMC information
provided in this operation manual.
^ Reference "8.1 Environmental Conditions of EMC (Electro-Magnetic Compatibility)" P.8-2
1
1
Check that the electromagnetic fields are compatible.

All peripheral devices must satisfy the EMC standards regarding emission of
electromagnetic waves and sensitivity to emitted electromagnetic waves.
Devices that do not satisfy these standards may disturb the correct
functioning of the system. In the worst case, this can cause serious injuries or
clinical errors.
1
1
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ix
Preface
MobileArt Evolution High Power Type (32 kW) should not be used
adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, MobileArt Evolution High Power Type
(32 kW) should be observed to verify normal operation in the configuration in
which it will be used.
Cautions on Radiation
Do NOT allow operation of this apparatus by any person other than

qualified personnel (physicians, radiotherapy engineers and clinical Xray engineers) or under observation by them.
Be aware of the potential for X-ray irradiation.

If X-ray equipment is not used correctly the operator, the subject, and other
persons may receive a greater dose of radiation than is necessary. Nobody
other than the subject should remain in the examination room during
irradiation. If for some reason another person has to be in the examination
room, that person must control X-ray irradiation from a distance over 2 m
from the focal spot and the X-ray beam and also must take adequate
measures to protect themselves against radiation.
During X-ray exposure, the status indicator lamp will illuminate, and a sound
is emitted.
M503-E027
Preface
1
1
In order to minimize the absorbed dose, make the focal spot to distance
as long as possible. (Minimum 45 cm)
1
1
Be sure to carry out aging before taking an X-ray radiograph.
Before taking an X-ray radiograph, running-in operation of the X-ray tube unit
called "aging" is required.
^ Reference "3.2 Aging the X-Ray Tube Unit" P.3-6
1
1
Avoid unnecessary standby situations.

In exposure, if a standby situation continues with the exposure ready key
pressed, wire disconnection or dielectric strength failure may result owing to
the vaporization of the X-ray tube filament.
1
1
After the X-ray tube unit is used for a long time at a relatively low tube
voltage (below 80 kV), if it is used in the range near the nominal highest
tube voltage (100 kV or more), discharge may result. This is an
accidental arc caused by the weakened aging effect at high tube voltage
after the X-ray tube unit is used for a long time at a lower tube voltage.
In this case, carry out the aging procedure described in Chapter 5
before operating the apparatus.
1
1
1
1
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xi
Preface
System Movement Cautions
When moving the arm unit or system, the operator must pay close
attention to ensure that the limbs of both operator and patient are not
caught between the system and any peripheral units.
Be especially careful when near a wall, changing the direction of the system
or moving it backwards.
Avoid collisions and overturning.

Collisions and overturning can not only damage the system, but can also
cause serious injury.
Be careful of the following points when moving the system:
When on a slope, in an entrance, or encountering obstacles, move the
system as slowly as possible. Be especially careful when descending/
ascending a steep slope.
Do NOT move the system on a slope steeper than 7 degrees or over steps
higher than 2 cm. When stopping the system, always park the system on a
level place, avoiding slopes, since there is a danger of the system rolling
down the slope and overturning.
Moving the system along surfaces that cause strong vibrations, such as
roads outdoors, over large steps and down steep slopes is dangerous.
Avoid these if possible. Do NOT stop the system on a slope.
When moving the system, look out for any obstacles in front of it.
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M503-E027
Preface
Scope of Software License (Only with FPD Upgrade)
1
1
Do NOT change any of the OS settings.
The system uses Windows XP as its operating system (OS). If the OS

settings are changed, the system operation is not guaranteed.
1
1.
Definition of licensed software

The licensed software ("software") refers to all computer programs
used by the system, in addition to all related documentation.
2.
Ownership of license
The software used in this system is copyrighted by Shimadzu
Corporation ("Shimadzu"), who possesses all rights, including
sublicenses for those rights (for copyrights, etc.) held by third parties.
The system with the installed software is sold on the basis of Shimadzu
licensing the software ownership to the customer. Accordingly, when
the customer uses the software, they must observe the items outlined
below:
(1) The customer shall only use the software for use with a single system.
(2) The intellectual property rights for the software are not transferred to the
customer.
(3) The customer, or any third party, is prohibited from performing any of the
following actions:
Duplicating the software.

Changing the software, in whole or part.
Transferring, loaning, or sublicensing the software.
Transferring the software outside Japan without the prior permission of the
Japanese or U.S. government.
1
1
1
1
M503-E027
xiii
Preface
Data Security (Only with FPD Upgrade)
xiv
If individual data stored in the system is either lost or destroyed, Shimadzu may
provide system maintenance to prevent future data loss. Shimadzu does not
guarantee the retrieval of any lost or damaged data.
Data stored in the system is always subject to the risk of loss or damage. Loss of
or damage to data may result from system failure or malfunction, and may also
arise as a result of the deterioration of part performance due to age. To avoid data
loss or damage, users are recommended to save all essential data to a hard
media, such as film, or store it on an external file system. Data stored on external
file systems are also subject to the risk of loss or damage. Regularly check the
contents of data stored on external file systems.
M503-E027
Preface
Precautions Regarding Connection with an External Device (Only
with FPD Upgrade)
1
1
Do NOT connect any other electrical device to the LAN connector and
the USB connector of the equipment except following electrical
devices:
Medical electrical devices which conform to IEC60601-1

Non-medical electrical devices which conform to related IEC safety
standards
Non-medical electrical devices which have safety equal to devices which

conform to IEC safety standards
In addition, please note the following:
1.
2.
When connecting medical electrical devices which conform to

IEC60601-1
Connect the equipment and a connected device with a common

protective ground, or connect an additional protective ground of the
connected device when that device is in a room not used for treatment
and diagnosis (office and storage room, etc.).
When connecting other electrical devices
(1) Connect an additional protective ground of the connected device, or

supply electrical power to the connected device from an isolated power
source when the connected device is in the room used for treatment and
diagnosis.
(2) Connect the equipment and a connected device with common protective
ground, or connect an additional protective ground of the connected
device when that device is in a room not used for treatment and diagnosis
(office and storage room, etc.).
Table.
Necessary measures when connecting electrical device to this equipment
Location of Connected Device
Connected Device
Diagnosis and Treatment Room
Medical electrical devices
which conform to
IEC60601-1
Other electrical devices
M503-E027
Other
Additional protective ground or

power supply from an isolated
power source
Common protective ground or

additional protective ground or
separation device
1
xv
Preface
Guarantee
The guarantee period of this system is one (1) year from the date of purchase.
Shimadzu bears no responsibility for loss of or damage to data, or for any of the failures or systemrelated damage due to the following reasons:
1.
Failure/damage caused by installation, movement, maintenance and

repair performed by anyone other than our company and companies
specified by our company.
2.
Failure/damage in a product of our company caused by a product of

other company which is not delivered by our company.
3.
Failure/damage based on maintenance, repair, etc. using a spare part

other than the genuine parts specified by our company.
4.
Failure/damage caused by natural disaster such as fire, earthquake,

flood and thunder.
5.
Installing the system in vehicles, ships, or aircraft, without Shimadzu's

permission.
6.
Use of the system in countries not specified by Shimadzu.
7.
Purchasing of the system from dealers other than Shimadzu or

Shimadzu's authorized distributors.
8.
Collisions, falls or strong impacts.
9.
Failure/damage caused by not following the cautions and operation

instructions described in this Operation Manual or in the Operation
Manual for Canon parts to be used for FPD upgrade.
10. Failure/damage caused by ambient or environmental conditions far from

the area of instrument usage (power source and installation
requirements) described in this Operation Manual or in the Operation
Manual for Canon parts to be used for FPD upgrade.
11. Failure/damage caused by installing software or connecting peripheral
devices not specified by Shimadzu if FPD is upgraded.
12. Failure/damage caused by changing or deleting the basic software's
configuration files (autoexec.bat, config.sys, etc.) or DR system specialuse files if FPD is upgraded.
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M503-E027
Preface
Shimadzu bears no responsibility for any failure or damage of the Canon CXDI-50G/50C/55G/55C/
60G/60C due to the following reasons, especially if FPD is upgraded.
1.
Hitting or dropping the CXDI-50G/50C/55G/55C/60G/60C sensor.
2.
One or more of the four shock detectors changed color to red.
3.
Overloading the unit beyond the specified range.
4.
Leakages of water, solutions, or large quantities of blood on the unit.
5.
Not following the operating procedure stipulated in the Operation

Manual.
6.
Use of the unit for purposes other than its intended use.
7.
Making alterations to the unit.
8.
Environmental pollution, fire, and natural disasters such as earthquakes,

flooding, lighting, as well as power supply problems.
1
1
1
1
1
1
The servicing after expiration of the guarantee period will be offered with charge.
Contact Shimadzu service representative nearest to you.
Service Life
The system's service life is 10 years (based on Shimadzu's criteria), and is limited to systems that
receive the prescribed maintenance checks. It is 7 years if FPD is upgraded.
1
1
1
1
1
1
M503-E027
xvii
Preface
Action for Environment (WEEE)

To all users of Shimadzu equipment in the European
Union:
Equipment marked with this symbol indicates that it was sold on or after 13th August 2005, which
means it should not be disposed of with general household waste. Note that our equipment is for
industrial/professional use only.
WEEE Mark
Contact Shimadzu service representative when the equipment has reached the end
of its life. They will advise you regarding the equipment take-back.
With your co-operation we are aiming to reduce contamination from waste electronic and electrical
equipment and preserve natural resource through re-use and recycling.
Do not hesitate to ask Shimadzu service representative, if you require further information.
xviii
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Preface
Warning and Caution Labels for Safety
Contents that require particular attention when handling this system are included in the following
safety labels which are attached to the system. These labels indicate potentially hazardous areas
where there is a danger of becoming physically caught in the system or where there is a risk of
optical damage from the projector. Together with the warning and caution items in this Operation
Manual, ensure that you have fully read and understood the contents of these safety labels to ensure
the safe operation of this system.
If the label for safety is peeled or unreadable due to stains or scratches, replace them with new ones.
For replacements, contact your Shimadzu service representative.
1
1
1
1
23
90
4
67
8
1
1
1
1
1
1
M503-E027
xix
Preface
xx
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Preface
With FPD Upgrade
1
1
1
23
1
89
6
4
5
1
1
1
1
1
1
1
1
1
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Preface
4
5
xxii
M503-E027
Contents
Contents
Preface
Precautions in Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iv
Be sure to Read the Safety Items to Prevent from Explosion
or Electric Shock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . v
Cautions on Use and Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . vii
Cautions on Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . viii
Cautions Relating to Cellular Telephones . . . . . . . . . . . . . . . . . . . . . . . .ix
Cautions on the Compatibility of Electromagnetic Fields . . . . . . . . . . . . .ix
Cautions on Radiation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . x
System Movement Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xii
Scope of Software License (Only with FPD Upgrade) . . . . . . . . . . . . . . xiii
Data Security (Only with FPD Upgrade) . . . . . . . . . . . . . . . . . . . . . . . . xiv
Precautions Regarding Connection with an External Device
(Only with FPD Upgrade) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xv
Guarantee . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .xvi
Service Life . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xvii
Action for Environment (WEEE)
To all users of Shimadzu equipment in the European Union: . . xviii
Warning and Caution Labels for Safety . . . . . . . . . . . . . . . . . . .xix
Chapter 1 Overview of MobileArt Evolution

1.1 Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
1.2 Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
1.3 Environmental Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
1.3.1
1.3.2
1.3.3
1.3.4
Operating Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Storage Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Grounding . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1-4
1-4
1-5
1-5
1.4 Classification of Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6

Protection Method Against Electric Shock . . . . . . . . . . . . . . . . . . . . . . 1-6
Degree of Protection Against Electric Shock . . . . . . . . . . . . . . . . . . . . 1-6
M503-E027
Contents-1
Contents
Operation Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6

Degree of Protection Against Liquid Ingress . . . . . . . . . . . . . . . . . . . . 1-6
Use in Flammable Atmosphere . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
1.5 Operator Profile . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7
Chapter 2 Part Names and Descriptions

2.1 External Appearance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
2.2 Grip Bar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Emergency Brake Release Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
2.3 Power Supply Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4

Status Indicator Lamp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.4 X-Ray Control Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6

2.5 Collimator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Status Indicator Lamp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
2.6 Hand Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10

2.7 Arm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
2.8 Apron Hanger . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
2.9 Power Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
2.10 Main Circuit Breaker and Additional Protective
Grounding Wire . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Main Circuit Breaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Additional Protective Grounding Wire . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Chapter 3 Basic Operation

3.1 Starting and Shutting Down the System . . . . . . . . . . . . . . . . . . 3-2
3.1.1 Starting the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
3.1.2 Shutting Down the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Auto-Power-OFF Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.2 Aging the X-Ray Tube Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6

Aging Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
3.3 Moving the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8

3.3.1 Travel Mode and Inch-Mover Buttons . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Normal Travel Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
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Low-Speed Travel Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Inch-Mover Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10
3.3.2 Obstruction Detector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Obstruction Detector Cancel Function . . . . . . . . . . . . . . . . . . . . . . . . 3-11
3.3.3 Emergency Stop Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
Releasing the Emergency Stop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
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3.4 Arm Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13

3.4.1 Locking and Releasing the Arm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Releasing the Arm Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Setting the Arm Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-14
3.4.2 Positioning the X-Ray Tube Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-15
3.4.3 Setting the Irradiation Field . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-17
Adjusting the Irradiation Field . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-17
Irradiation Field Reference Light . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-18
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3.5 Setting the Radiography Parameters . . . . . . . . . . . . . . . . . . . 3-19

3.5.1 Setting the Radiography Parameters . . . . . . . . . . . . . . . . . . . . . . . . . 3-19
3.5.2 Setting the Radiography Parameters
Using the Anatomical Programs (APR) . . . . . . . . . . . . . . . . . . . . . . . 3-19
Selecting an Anatomical Program for Cassette Radiography Mode . 3-19
3.5.3 Manually Setting the Radiography Parameters . . . . . . . . . . . . . . . . . 3-20
Setting the X-ray Tube Voltage (kV) . . . . . . . . . . . . . . . . . . . . . . . . . 3-20
Setting the Current-Time Product (mAs) . . . . . . . . . . . . . . . . . . . . . . 3-20
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Changing the Focal Spot . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-20
3.6 X-Ray Radiography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-21

3.6.1 Cassette Radiography Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-22
3.6.2 Low-Battery Radiography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24
Current-Time Product Limits for Low Battery Voltage . . . . . . . . . . . . 3-24
3.6.3 Additional Radiography Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25
3.7 Charging the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-26
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Charging After Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-27

Charging Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-27
Chapter 4 Advanced Operation
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4.1 User Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2

4.1.1 Entering the User Settings Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Registering Changed Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Not Registering Changed Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
4.1.2 Personal ID Setting [Pid] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
4.1.3 Power-Assist Setting [PAS] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
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Contents
4.1.4 Acceleration Setting [Acc] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4.1.5 Steer Control Setting [stc] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.1.6 Backward Power-Assist Setting [bAC] . . . . . . . . . . . . . . . . . . . . . . . . .
4.1.7 Auto-Power-Off Time Setting [APO] . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.1.8 Buzzer Setting [bon] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.1.9 Collimator Lamp Control Setting [LAP] . . . . . . . . . . . . . . . . . . . . . . . .
4.1.10APR Settings at Startup [aPr] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4.1.11Operation Sound Setting [Snd] . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Pattern Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4-5
4-5
4-6
4-6
4-7
4-7
4-8
4-9
4-9
Setting the Pattern Tone . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9

Setting the Sound Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Setting the sound emitted during X-ray exposure. . . . . . . . . . . . . . . . 4-10
Setting the sound emitted when radiography preparation is finished. 4-11
Setting the sound emitted during system travel . . . . . . . . . . . . . . . . . 4-11
Checking the Sound Pattern . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
4.2 Changing the Operation Sound Volume . . . . . . . . . . . . . . . . . 4-12

Changing the Sound Volume Emitted During X-Ray Exposure
or When Radiography Preparation Is Finished . . . . . . . . . . . . . . . . . 4-12
Using the Collimator Lamp Button to Adjust Volume . . . . . . . . . . . . . 4-13
4.3 Changing Anatomical Program Parameters . . . . . . . . . . . . . . 4-14

4.3.1 Registering Anatomical Programs . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
Registration Procedure for Cassette Radiography . . . . . . . . . . . . . . . 4-14
4.3.2 Deleting Unused Anatomical Programs . . . . . . . . . . . . . . . . . . . . . . . 4-15
Deleting Unused Anatomical Programs . . . . . . . . . . . . . . . . . . . . . . . 4-15
How to Use the Deleted Anatomical Program . . . . . . . . . . . . . . . . . . 4-16
4.4 Releasing the Brake in Emergency . . . . . . . . . . . . . . . . . . . . . 4-17

4.4.1 Activating the Brake Release Function . . . . . . . . . . . . . . . . . . . . . . . 4-17
4.4.2 Releasing the Brake in Emergencies . . . . . . . . . . . . . . . . . . . . . . . . . 4-17
4.5 Notification Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-18

Confirming the Usage Period, Count and Distance Information
for Each Part . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-19
Temporarily Disabling the Replacement Time Display Function . . . . 4-20
Chapter 5 Optional Features

5.1 Remote Controller . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Using the Remote Controller . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Operable Range of the Remote Controller . . . . . . . . . . . . . . . . . . . . . . 5-4
Replacing Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
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5.2 Protective Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Using the Shield . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
5.3 Dose Area Product Meter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Using the Dose Area Product Meter . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7

Cleaning the Dose Area Product Meter . . . . . . . . . . . . . . . . . . . . . . . . 5-8
5.4 Dose Calculation Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Using the Dose Calculation Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
5.5 Distance Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11

5.6 Keyless Entry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
5.7 Changing the Grip Bar Height . . . . . . . . . . . . . . . . . . . . . . . . . 5-14

5.8 Luminous Hand Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
Using the Hand Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
5.9 Additional Hand Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16

5.10 Grid Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-17
5.11 Large Cassette Box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-18
5.12 FPD Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-19
Chapter 6 Troubleshooting
6.1 Warning Indicator Lamp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
6.2 Malfunction Indicator Lamp . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4

6.3 Storing the System for a Long Period . . . . . . . . . . . . . . . . . . . . 6-5
Storage Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Chapter 7 Maintenance and Inspection
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7.1 Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2

7.1.1 Daily Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
7.1.2 Periodic Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
7.2 Cleaning the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7

7.3 Periodic Replacement Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
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Chapter 8 Specifications
8.1 Environmental Conditions of EMC
(Electro-Magnetic Compatibility) . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Classification of EMI in Accordance with EN/IEC 60601-1-2: 2001 . . . 8-2
Performance to Be EMC Immunity Tested (Essential Performance) . . 8-2
Cable List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Option List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Guidance and Manufacturer's Declaration
- Electromagnetic Emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
- Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
- Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Recommended Separation Distances between Portable and Mobile
RF Communications Equipment and the EQUIPMENT or SYSTEM . . 8-7
8.2 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8

8.2.1 Operating Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
8.2.2 Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
8.2.3 High-Voltage Generator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
8.2.4 X-ray Tube Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
8.2.5 Collimator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12
8.2.6 X-ray Tube Unit Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12
8.2.7 Minimum Inherent Filtration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-13
8.2.8 DR System (Only with FPD Upgrade) . . . . . . . . . . . . . . . . . . . . . . . . 8-13
8.2.9 Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-14
8.2.10Custom Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-15
8.3 Dimensional Drawings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-16

8.3.1 General Dimensions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-16
8.4 X-Ray Tube Unit Reference Axis and Focal Spot Position . . . 8-18
8.5 Radiography Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-19
8.5.1 Normal Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-19
Large Focus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-19
Small Focus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-20
8.5.2 Low-Battery Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-21
Large Focus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-21
Small Focus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-22
8.6 Anatomical Program . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-23

8.6.1 Anatomical Program . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-23
8.6.2 Anatomical Program Number (Only with FPD upgrade) . . . . . . . . . . 8-26
8.7 Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-37
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Product Name Plates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-38
Warning Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-40
Indication Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-41
Other Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-41

8.7.1 Labeling For X-Ray Tube Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-42
Name Plates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-42
Warning Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-42
Indication Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-43

Other Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-43
8.8 Statement of Compliance [For Europe] . . . . . . . . . . . . . . . . . . 8-44

8.8.1 Regulatory Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-44
8.8.2 Company's Quality System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-44
8.8.3 International Standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-45
8.9 Manufacturer Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-46
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Chapter 9 FPD Upgrade

9.1 Overview of FPD Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
9.1.1 Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
9.1.2 Environmental Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
9.2 Part Names and Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
9-3
9-5
9-6
9-8
9.2.4 Storage Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-10

One Imaging unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-10
9.2.1 Power Supply Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9.2.2 Disposable Wipes Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
9.2.3 CXDI-50G/50C/55G/55C/60G/60C Imaging Unit . . . . . . . . . . . . . . . . .
Cautions Relating to CXDI-55G/55C/60G/60C . . . . . . . . . . . . . . . . . .
Two Imaging Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-11

9.2.5 LAN Connector for External Connection . . . . . . . . . . . . . . . . . . . . . . 9-11
9.3 Basic Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-12

9.3.1
9.3.2
9.3.3
9.3.4
9.3.5
Starting and Shutting Down the System . . . . . . . . . . . . . . . . . . . . . .

Aging the X-ray Tube Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Moving the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Arm Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Setting the Radiography Parameters . . . . . . . . . . . . . . . . . . . . . . . . .
Selecting an Anatomical Program for DR Radiography Mode . . . . . .
9-12
9-12
9-12
9-12
9-13
9-13
Changing to the Cassette Radiography Mode . . . . . . . . . . . . . . . . . . 9-13

Selecting an Anatomical Program for Cassette Radiography Mode . 9-13
1
1
1
Manually Setting the Radiography Parameters . . . . . . . . . . . . . . . . . 9-13

9.3.6 X-ray Radiography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-14
1
M503-E027
Contents-7
Contents
DR Radiography Procedure
(Changing to the DR Radiography Mode) . . . . . . . . . . . . . . . . . . . . . 9-14
Transferring Images to an External Printer or PACS System . . . . . . 9-17
Saving Images to External Media . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-18
Cassette Radiography Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-18
9.4 Advanced Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19

9.4.1 Registering Anatomical Programs . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19
Registration Procedure for DR Radiography . . . . . . . . . . . . . . . . . . . 9-19
Registration Procedure for Cassette Radiography . . . . . . . . . . . . . . . 9-21
9.4.2 Deleting Unused Anatomical Programs . . . . . . . . . . . . . . . . . . . . . . . 9-22
Deleting Unused Anatomical Programs . . . . . . . . . . . . . . . . . . . . . . . 9-22
How to Use the Deleted Anatomical Program . . . . . . . . . . . . . . . . . . 9-22
9.5 Optional Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-23

9.5.1 Grid Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-23
9.5.2 Wireless LAN Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-24
Using a Wireless LAN Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-24
Wireless LAN Adapter Specifications . . . . . . . . . . . . . . . . . . . . . . . . . 9-24
9.5.3 Second FPD Kit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-25
Using the Sensor Unit Attach/Detach Function . . . . . . . . . . . . . . . . . 9-25
Storage case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-27
9.5.4 FPD Bag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-28
Appendix
Check List for Trouble . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . App-2
Safety Check Registry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . App-3
Index
Contents-8
M503-E027
Chapter
Overview of
MobileArt Evolution
1
J Contents
1.1
Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2
1.2
Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
1.3
Environmental Conditions . . . . . . . . . . . . . . . . . . . . . . .1-4
1.4
Classification of Equipment . . . . . . . . . . . . . . . . . . . . . .1-6
1.5
Operator Profile . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7
1 Overview of MobileArt Evolution High Power Type (32 kW)
1.1
Applications
The MobileArt Evolution High Power Type (32 kW) is a general purpose mobile digital X-ray
system, which can be moved freely throughout a hospital to directly obtain X-ray images of various
areas of the body.
Do NOT use the system for any other purpose than indicated above.
Do NOT connect the system to any other equipment, either by electrical
or mechanical means, or modify the system.
1-2
M503-E027
1.2 Features
1.2
Features
Smooth and Quiet Movement
Power-assisted technology allows moving the system easily and quietly.
Compact Design
Excellent forward visibility allows moving freely through even tight spaces.
Easy Positioning
The system can be freely and quickly maneuvered into position using the Inch-Mover buttons to
move the main body and to swivel the column to move the X-ray tube unit.
High Frequency Inverter

Using a high-frequency inverter which generates high voltage (with a maximum frequency of
60 kHz) provides efficient X-ray generation with low-ripple distortion.
Standard Anatomical Programs

Anatomical programs (APR) are installed as standard, to easily allow setting radiography
parameters.
Cordless System
The built-in battery enables the obtaining of X-ray images without plugging in the system.
Status Indicator Lamp
The status indicator lamp illuminates or blinks in response to X-ray exposure or system
abnormalities. This allows a visual confirmation of the system status.
FPD Upgrade
If the DR system is equipped, the DR radiography can be made available.

^ Reference "9 FPD Upgrade" P.9-1
Immediate Response
A reference image appears on the display in about 3 seconds, allowing on-site image confirmation.
High Throughput
Improves workflow by eliminating the need to prepare a cassette, develop images, or read CR plates,
and by the hospital internal network to send image data to an imager or PACS.
1
1
1
1
M503-E027
1-3
1.3
Environmental Conditions
Charge the battery under conditions described in "1.3.1 Operating

Environment" P.1-4, not "1.3.2 Storage Environment" P.1-4.
1.3.1
Operating Environment
Item
1.3.2
Specifications
General
The equipment which is used in hospitals, corridor, patient

room etc.
Condition of visibility
Ambient brightness is 100 lx min., 800 lx max.
Ambient Temperature
Relative Humidity

(with no condensation)
Atmospheric Pressure
700 hPa to 1060 hPa
Frequency of use
15000 exposures / year
Storage Environment
Item
1-4
Specifications
Ambient Temperature
-10 C to 40 C
Relative Humidity

700 hPa to 1060 hPa
M503-E027
1.3 Environmental Conditions
1.3.3
Power Supply
AC Power
Item
Phase
Single phase AC
Frequency
50/60 Hz
Standard Voltages
100, 110, 120, 200, 220, 230, 240 V

(Set to one of the voltages when installing)
Voltage Fluctuation Range
10% of nominal voltage
Supply Capacity
1 kVA
Power Supply Impedance
1.3.4
Specifications
100, 110, 120 V:
Max. 1.0
200, 220, 230, 240 V:
Max. 4.0
1
1
1
1
Grounding
Ground Terminal:
Max. ground resistance: 100
Additional Ground Terminal: Max. ground resistance: 100
1
1
1
1
1
1
1
M503-E027
1-5
1.4
Classification of Equipment
This system is classified as follows, based on safety standards for electrical medical equipment.
J Protection Method Against Electric Shock

Class I equipment (when connected by the power supply plug)
Internally-powered equipment (when powered by the battery)
J Degree of Protection Against Electric Shock

Type-B equipment
J Operation Mode
Continual operation with intermittent loading
J Degree of Protection Against Liquid Ingress

Ordinary equipment
J Use in Flammable Atmosphere

Not to be used in presence of flammable anaesthetic gas
Using this system in the presence of flammable anaesthetics gas risks

causing an explosion.
1-6
M503-E027
1.5 Operator Profile
1.5
Operator Profile
Item
Details
Age
Age that person can obtain the license of Radiologic Technologist or a

license equal to it.
Sex
No limitation
Nationality
No limitation
Education
Radiologic Technologist or person who is licensed with equal

qualifications.
Knowledge
Radiologic Technologist or person who is licensed with equal

qualifications.
Language
Can read and understand English.
1
1
1
Necessary.
Experience
Permissible impairments
Others
Every operator needs to take training for operating the equipment

before using it.
Minimum of 0.7 visibility (corrected vision with lenses acceptable).
No serious physical impairments in general health or extremities.

Minimum height of 140 cm to ensure clear visibility ahead of
equipment during transport.
1
1
1
1
1
1
1
M503-E027
1-7
Chapter
Part Names and

Descriptions
J Chapter Contents
2.1
External Appearance . . . . . . . . . . . . . . . . . . . . . . . . . .2-2
2.2
Grip Bar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
2.3
Power Supply Panel . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
2.4
X-Ray Control Panel . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6
2.5
Collimator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
2.6
Hand Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-10
2.7
Arm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
2.8
Apron Hanger . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12
2.9
Power Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-13
2.10 Main Circuit Breaker and Additional Protective Grounding

Wire . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-14
2 Part Names and Descriptions
2.1
External Appearance
Column
X-ray Tube
Unit
Arm (P.2-11)
Arm Joint (P.2-11)
Power Supply Panel and Touch Panel Monitor
(P.2-4)
X-ray Control Panel (P.2-6)
Collimator (P.2-8)
Grip Bar (P.2-3)
Hand Switch
(P.2-10)
Main Circuit Breaker
(P.2-14)
2-2
M503-E027
2.2 Grip Bar
2.2
Grip Bar
This bar is used to move the system. Squeezing the brake release bar releases the brake and allows
pushing or pulling the system in the desired direction.
Grip Bar
2
2
2
Brake Release Bar
2
Do NOT touch the brake release bar unless intending to move the
system.
Doing so will release the brake, allowing the system to move unexpectedly.
J Emergency Brake Release Button

When an accident occurs and the power-assist does not function, the brake can be released, allowing
users to manually move the system.
^ Reference "4.4 Releasing the Brake in Emergency" P.4-17
Emergency Brake Release Button
2
2
2
2
M503-E027
2-3
2.3
Power Supply Panel

1
3
6
No.
Name
Function
Key Switch
Battery Indicator
Normally indicates the amount of energy remaining in the battery, but

also indicates charging status during battery recharging.
Power Line Connection

Indicator Lamp
Illuminates when connected to a power outlet.
Charging Lamp
Emergency Stop Button
Indicates system status by blinking or changing color.

Turning the key switches system power ON
The key can be removed only in the OFF
or OFF
position.
Blinks when battery is being charged.

Illuminates when charging is complete.
Used to stop travel movement in an emergency situation.
2-4
^ Reference "3.3.3 Emergency Stop Button" P.3-12
Documents and other papers can be put on the power supply panel.
Do not place more than a total weight of 1 kg on the power supply panel.
M503-E027
2.3 Power Supply Panel
J Status Indicator Lamp
The status indicator lamp changes color in the following sequence, according to system status.
System Preparation
in Progress
(after starting the system)
Light OFF
System
Preparation
Finished
Preparing for
Radiography
Blue light
Green light blinking
(arm is released)
Radiography
Preparation
Finished
Radiography
in Progress
System Preparation
in Progress
(after radiography)
Error
Detected
Green light
Orange light
Blue light blinking

(returns to blue light)
Red light
2
2
2
If the status indictor lamp is red, the code is displayed on the mAs
display on the X-ray control panel. If the status indicator is red, please
carefully read "6 Troubleshooting" P.6-1 and take the appropriate
measures.
2
2
2
2
2
2
2
2
2
M503-E027
2-5
2.4
X-Ray Control Panel

1
6
16
7
17
8
18
15 14
No.
Description
13
Display/
Button
12
11
10
Function
Radiography Ready
Indicator Lamp
Illuminates when ready for radiography.
X-ray Irradiation
Indicator Lamp
Illuminates whenever X-rays are being emitted.
Standby Indicator
Lamp
Illuminates when the system is ready to prepare for X-ray

radiation.
Warning Indicator
Lamp
Illuminates when the system does not function correctly.
Malfunction Indicator
Lamp
Illuminates if system malfunctions.
Travelling Warning
Sound
Enables you to set the volume of the sound emitted during

X-ray exposure or when radiography preparation is finished.
Cassette Mode:
Normally left LED illuminated
FPD/Cassette
Radiography Mode
Button
FPD Mode:
Right LED illuminated or blinked
Focus Mode Button
Collimator Lamp
Button
(FPD radiography mode can be selected if FPD is upgraded).

Changes focus of the X-ray tube. Toggles between large and
small focuses with each press, where illuminated LED
indicates small focus.
Switches collimator lamp ON or OFF. Also used in
combination with the key switch for obstruction detector
canceling function.
^ Reference "3.3.2 Obstruction Detector" P.3-11
2-6
10
Remote Controller
Button
Switches between infrared remote controller enabled (LED

ON) and disabled (LED OFF) modes.
11
DR Long-Term
Exposure Button
LED illuminates when DR long-term exposure mode is

selected. (This can be used if FPD is upgraded).
M503-E027
2.4 X-Ray Control Panel
Display/
Button
No.
Description
Function
12
mAs Display /
Current-Time Product
Buttons
Displays mAs setting. Pressing buttons sets the current-time

product.
13
kV Display / Tube
Voltage Buttons
Displays kV setting. Pressing buttons sets the tube voltage.
14
User Settings Button
^ Reference "4.1 User Settings" P.4-2
15
Registration Button
Registers anatomical programs and user settings
2
2
2
Selects imaging of the head region (head, face, nose, ear,

neck, etc.).
Selects imaging of the chest region (collarbone, ribs,

shoulder blade, thoracic spine, etc.).
Selects imaging of the abdomen region (abdomen, lumbar,
etc.).
16
Imaging Region
Selection Buttons
Selects imaging of the waist region (pelvis, coccyx, fetus,

femur, etc.).
Selects imaging of the leg region (knee, shin, etc.).

Selects imaging of the foot region (heel, foot, toes, etc.).
Selects imaging of the arm region (upper arm, elbow, wrist,
etc.).
Selects imaging of the hand region (hand, fingers, etc.).
Selects frontal projection.

17
Projection Direction
Selection Buttons
Selects lateral projection.
Selects oblique projection.

Selects Thin.
18
Body Thickness
Selection Buttons
Selects Normal.
Selects Thick.
2
2
M503-E027
2-7
2.5
Collimator
1
2
3
4
5
6
No.
1
2
Description
Function
Arm Lock Release Buttons
Pressing the arm lock release button unlocks the column rotation,
vertical X-ray tube unit movement, and arm extension/contraction.
(All Free button)
Inch-Mover Buttons
When the arm is unlocked, pressing the inch-mover buttons will move
the system forward or backward in small increments (about 5 cm/s).
When the arm is locked, the inch-mover buttons are non-functional.
Irradiation Field Adjustment

Knobs
Adjusts the size of the irradiation field.
Tape Measure
Used to measure SID (distance between focal spot and cassette or

imaging unit).
Collimator Lamp Button
Used to switch the collimator lamp ON or OFF. It has the same

function as the
(collimator lamp button) on the X-ray control
panel.
When the arm is locked, switches moving alarm ON or OFF.
2-8
M503-E027
2.5 Collimator
J Status Indicator Lamp
The status indicator lamp changes color in the following sequence, according to system status.
System Preparation
in Progress
(after starting the system)
Light OFF
System
Preparation
Finished
Preparing for
Radiography
Blue light
Green light blinking
(arm is released)
Radiography
Preparation
Finished
Radiography
in Progress
System Preparation
in Progress
(after radiography)
Error
Detected
Green light
Orange light
Blue light blinking

(returns to blue light)
Red light
2
2
2
If the status indictor lamp is red, the code is displayed on the mAs
display on the X-ray control panel. If the status indicator is red, please
carefully read "6 Troubleshooting" P.6-1 and take the appropriate
measures.
2
2
2
2
2
2
2
2
2
M503-E027
2-9
2.6
Hand Switch
1
No.
Name
Radiography Preparation
Button
(pushed to first level)
Function
When held down, the radiography ready indicator lamp illuminates to
indicate that the system is finished preparing for radiography. Pressing
and immediately releasing the button allows switching the collimator
lamp ON and OFF.
^ Reference "3.4.3 Setting the Irradiation Field" P.3-17
2-10
X-Ray Exposure Button

(pushed to second level)
When this button is pressed, while the standby indicator lamp is

illuminated, radiography can be performed.
M503-E027
2.7 Arm
2.7
Arm
2
1
2
3
2
No.
1
2
Name
Arm Lock Release Button
Function
(All Free button)
Pressing the arm lock release button unlocks the column rotation,
vertical X-ray tube unit movement, and arm extension/contraction.
Arm Joint
Mechanism that holds the X-ray tube unit.
Arm Lock Release Lever
This lever has the same function as the arm lock release button. It
allows unlocking the arm by lifting up the X-ray tube unit while
holding the arm lock release lever down.
2
2
2
2
2
2
2
M503-E027
2-11
2.8
Apron Hanger
This hanger is used for hanging X-ray protective aprons.
.
Apron Hanger
Use the apron hanger only for hanging aprons.

Do NOT hang objects over 7 kg on each apron hanger.
Do NOT hang an apron on the apron hanger when the arm is not
locked.
Move the system carefully if an apron is on the apron hanger,
especially when moving the system over any changes in floor level
or on slopes.
2-12
M503-E027
2.9 Power Cable
2.9
Power Cable
Use when the battery charging.
Move the system to a nearby outlet, pull out the power plug from the front of the system and insert it
into the power outlet.
When pulling out the power cable, the cable is held within the range to where click sound from the
cable reel can be heard. The cable is rewound in the range where no sound from the cable reel can be
heard.
2
2
2
Power Cable
2
2
2
When pulling out the power cable, hold the plug portion and do NOT
apply excessive force to the cable.
Excessive force may damage the cable or internal cable reel.
2
2
When rewinding the cable, hold the plug until it is completely

retracted.
2
2
2
2
M503-E027
2-13
2.10Main Circuit Breaker and Additional Protective

Grounding Wire
Additional Protective
Grounding Wire
ON
OFF
J Main Circuit Breaker

The main circuit breaker opens or closes the connection between the battery and internal circuits.
If an overcurrent flows from the battery, the main circuit breaker detects the overcurrent and
automatically switches OFF.
If the main circuit breaker switches OFF frequently, stop using the
system and contact your Shimadzu service representative.
2-14
Keep the main circuit breaker switched OFF when not using the system for any
long period of time.
The system can not be used when the main circuit breaker is turned OFF.
If the main circuit breaker is switched OFF while the key switch is turned ON, the
connection between the battery and the internal circuits is closed, and the system
may remain ON for some time due to the residual charge within the internal
circuits.
M503-E027
2.10 Main Circuit Breaker and Additional Protective Grounding Wire
J Additional Protective Grounding Wire
2
2
While charging, Shimadzu recommends connecting the additional protective

grounding wire to a grounding terminal with a grounding resistance of 100 or less.
2
2
2
2
2
2
2
2
2
2
2
M503-E027
2-15
Chapter
Basic Operation
J Chapter Contents
3.1
Starting and Shutting Down the System . . . . . . . . . . . .3-2
3.2
Aging the X-Ray Tube Unit . . . . . . . . . . . . . . . . . . . . . .3-6
3.3
Moving the System . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
3.4
Arm Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-13
3.5
Setting the Radiography Parameters . . . . . . . . . . . . .3-19
3.6
X-Ray Radiography . . . . . . . . . . . . . . . . . . . . . . . . . . .3-21
3.7
Charging the Battery . . . . . . . . . . . . . . . . . . . . . . . . . .3-26
3 Basic Operation
3.1
3.1.1
Starting and Shutting Down the System

Starting the System
To start the system, turn the key switch to the ON
position.
The system confirms its functions before the remaining battery charge is indicated on the battery
indicator. After the battery charge status has been indicated, the system can be moved, the arm lock
released, X-ray radiography operations performed or the DR system (only with FPD upgrade)
started. When the
(standby indicator lamp) is illuminated, radiography can be performed. The
following limits are placed on X-ray radiography depending on the remaining battery charge display.
No.
Battery Indicator
X-ray Radiography Availability

Radiography is possible.
Low Battery - only low-battery radiography is possible.
Blinking
^ Reference "3.6.2 Low-Battery Radiography" P.3-24
Radiography is not possible.

^ Reference "3.7 Charging the Battery" P.3-26
Indicator segment is illuminated if shown in black J and off if shown in white F above.
If the battery indicator is blinking, immediately charge the battery.
3-2
M503-E027
3.1 Starting and Shutting Down the System
The
(standby indicator lamp) will illuminate almost immediately if restarting
the system directly after shutting it down; It may take as long as one minute to
illuminate if restarting after the system has not been performed over a long period
of time.
If the key switch is turned ON

with buttons or levers left ON, code d4 to d11
appears on the mAs display. Release the switch or lever.

with the hand switch still depressed, code F64
or F65 appears on the mAs display. Release the hand switch.
Please note that the battery voltage rises temporarily immediately after the key
switch is turned ON
. As a result, the battery indicator will indicate more than
the actual remaining charge. After the system is used for a while, the battery
display will return to its actual remaining charge.
3
3
3
3

with the emergency stop button still depressed,
code F6d appears on the mAs display.
If the emergency stop button is reset after the key switch is turned ON
with
the emergency stop button in the pressed state, code d13 will appear and the
system will lock tight. In this case, restart the system while the emergency stop
button is in the reset state.
* It is possible to change the APR indicated when starting the system.
3
3
3
See "4.1 User Settings" P.4-2.
3
3
3
3
3
M503-E027
3-3
3 Basic Operation
3.1.2
Shutting Down the System

To shut down the system, turn the key switch to the OFF
3-4
position.
Always turn the key switch to OFF

system unattended.
and remove the key when leaving the
Even with key switch in the OFF

position, the DR system will not be shut
down. Be sure to shut down the DR system when leaving the system unattended
(only with FPD upgrade).
When not using the system for a long period of time, turn the main circuit breaker
to OFF.
M503-E027
3.1 Starting and Shutting Down the System
J Auto-Power-OFF Function
When the key switch is ON
, the auto-power-off function shuts the system off if not used for a
long time. The auto-power-off function default setting is 15 minutes. When the auto-power-off
function starts up, [at OFF] is displayed on the X-ray control panel until the system is shut off. When
the power plug is connected, [at OFF] will not disappear even if the system is shut off.
To reset from the auto-power-off condition, turn the key switch OFF
turn it back ON
.
, wait three seconds, then
3
3
3
* The time setting can be changed if necessary.

When the auto-power-off function is started with the connection of the power plug,
disconnect the power plug to restart the system.
When the system is used by connecting the power plug, deactivate the autopower-off function or set the auto-power-off time to 30 minutes.
Even if the auto-power-off function shuts the system off, the battery will continue
to consume a small amount of power. When the system is not in use, turn the key
switch to OFF
.
If the battery indicator displays no illuminated portion, the auto-power-off function

will automatically start in 5 minutes to prevent wearing out the battery.
The auto-power-off function does not turn the DR system OFF (only with FPD
upgrade).
If the system is left with the DR system still running, the battery will continue to
consume a small amount of power. Therefore, always turn the DR system OFF
when the system is not in use (only with FPD upgrade).
3
3
3
3
3
3
3
3
3
M503-E027
3-5
3 Basic Operation
3.2
Aging the X-Ray Tube Unit

X-ray tube units must be aged before they can be used. Always age the X-ray tube unit prior to using
the system.
Always age the X-ray tube unit before starting radiography. In

particular, if X-ray tube voltage is set to over 100 kV, aging should be
performed on a daily basis.
Performing radiography without aging the X-ray tube unit may cause an
electrical discharge.
J Aging Procedure
Usage Condition
Aging Description
Aging 1
When using the X-ray tube unit for the

first time that day
When the X-ray tube voltage to be used

is 100 kV or higher
When the X-ray tube voltage to be used
is 100 kV or higher, after normally
using a voltage of 80 kV or less
3-6
Generate X-rays, starting with the parameters indicated for Step 1

below, then successively generate X-rays indicated for each step,
until reaching the X-ray tube voltage to be actually used. If anything
abnormal occurs, go back two steps and repeat the process.
Aging 2
Start generating X-rays at Step 3 and successively increase steps
until reaching the X-ray tube voltage to be actually used. If anything
abnormal occurs, go back two steps and repeat the process.
M503-E027
3.2 Aging the X-Ray Tube Unit
Aging Procedure
Step
Tube Voltage (kV)
(mAs)
60
10
40
70
10
40
80
10
40
90
10
40
100
10
40
110
10
40
115
10
40
120
10
40
125
10
40
10
130
10
40
11
133
10
40
Number of Times
Pause (seconds)
3
3
3
3
3
3
3
3
3
3
3
3
M503-E027
3-7
3 Basic Operation
3.3
Moving the System
To move the system, hold the grip bar securely.

Do NOT operate the grip bar with only one hand or underhanded. Doing so
can result in not only operation errors and system damage, but also a serious
accident leading to injury or death.
If the battery indicator is not illuminated, immediately charge the

battery.
Do NOT touch the brake release bar unless intending to move the
system.
Doing so will release the brake, allowing the system to move
unexpectedly.
^ Reference "2.2 Grip Bar" P.2-3
If the system moves abnormally, immediately stop using the system

and contact your Shimadzu service representative.
The operator may experience static electric shock when moving the system if
their body has become statically charged, depending on conditions such as
humidity and type of clothing.
3-8
M503-E027
3.3 Moving the System
3.3.1
Travel Mode and Inch-Mover Buttons
3
3
When moving the system, make sure that there are no obstacles
ahead.
The obstacle detector may not be able to detect light weight obstacles in
front of it, such as IV stands or cables from other equipment. Hitting an IV
stand or running over cables from other equipment could be very
dangerous to patients.
Do NOT move the system over any steps or bumps greater than 2 cm,
or slopes steeper than 7 degrees.
Always stop the system on a level surface and avoid sloped surfaces.
Failure to do so may cause the system to roll down the slope or tip over.
Do NOT operate this system outdoors.
This system is designed for indoor use only. Using this system outdoors
may lead to system failure.
3
3
3
The system can be moved using the normal travel mode, low-speed travel mode, or inch-mover
buttons.
By squeezing the brake release bar on the lower surface of the grip bar and pushing on the bar, the
system moves in the direction it is pushed. In addition, the system's power-assist technology allows
changing the travel speed according to how much force is applied.
3
3
J Normal Travel Mode

The system is in the normal travel mode when the arm is locked.
^ Reference "3.4.1 Locking and Releasing the Arm" P.3-13
Maximum speed is about 5 km/h.
* Travel characteristics can be changed.
J Low-Speed Travel Mode

If the arm is not locked, the system will automatically select the low-speed travel mode.
3
3
M503-E027
3-9
3 Basic Operation
The traveling speed of the system will be limited to about half the normal speed and the degree of
power-assist is limited to about half of its normal level.
Do Not move the system over bumps or other floor-level changes in

low-speed travel mode.
The system may tip over if the arm is not locked.
Do Not move the system over slopes steeper than 5 degrees.
J Inch-Mover Buttons
Holding down the inch-mover buttons with the arm unlocked allows the movement of the system
forward or backward more slowly than in the low-speed travel mode. Maximum speed is about 5 cm/
s.
The inch-mover buttons can be operated continuously for about 10 seconds.
To continue using the buttons, press them again.
Motor power is lower than in the low-speed travel mode. If the system cannot be moved due to thickpiled carpet, or other resistance, use the grip bar.
The system does not move if both inch-mover buttons are pressed simultaneously, or pressing one of
the buttons while the other is already pressed.
Inch-Mover Button
(moves forward)
Inch-Mover Button
(moves backward)
If the system does not stop due to inch-mover button failure, stop the
system by pressing the emergency stop button on the power supply
panel.
3-10
M503-E027
3.3 Moving the System
3.3.2
Obstruction Detector
The obstruction detector is located at the lower front part of the system. If the obstruction detector
hits an obstacle, the system will stop and the unit can only be moved backwards.
* The obstruction detector can be set to emit a sound if activated.

3
3
3
3
J Obstruction Detector Cancel Function

If the obstruction detector is damaged, the obstruction detection function may remain ON (activated).
In this case, the obstruction detector cancel function can be used to temporarily cancel the
obstruction detector function, allowing the system to be moved.
3
3
The obstruction detector cancel function is only a temporary

measure. If the obstruction detector does not function normally,
contact your Shimadzu service representative.
While the obstruction detector cancel function is enabled, the

detector will not emit any sound, even if activated. Because there is
no auditory warning, be sure to pay careful attention to the area in
the periphery of the system while moving.
After moving to a safe location, disable the obstruction detector

cancel function.
1
2
Turn the key switch to OFF
Turn the key switch ON

while pressing the
button) on the X-ray control panel.
(collimator lamp
* The obstruction detector cancel function is disabled when the key switch is turned to the OFF
position. To enable this function again, repeat Step 2 above.
M503-E027
3-11
3 Basic Operation
3.3.3

To stop system movement in an emergency, press the emergency stop button on the power supply
panel.
Radiography is not possible when the emergency stop button is depressed.
Emergency Stop
Button
If you press the emergency stop button due to abnormal behavior of the
system, stop all operations and contact your Shimadzu service
representative.
When the emergency stop button is pressed, turn the key switch to OFF
, and move the system to a safe location using the emergency brake
release function.
^ Reference "4.4.2 Releasing the Brake in Emergencies" P.4-17
J Releasing the Emergency Stop

To release the emergency stop button, if you have pressed it accidentally or pressed it for testing, turn
the key switch to OFF
and turn the emergency stop button in the direction of the arrow.
Emergency Stop
Button
3-12
M503-E027
3.4 Arm Operation
3.4
3.4.1
Arm Operation
Locking and Releasing the Arm
The arm is in the locked position when the arm and the main unit are coupled at the arm joint section.
During radiography, the arm lock is released to allow the movement of the X-ray tube unit to the
imaging position.
3
3
Do NOT release the arm lock if the unit is on a slope greater than 5
degrees.
The system may tip over if the arm is rotated, extended/contracted, or moved
up or down on a slope greater than 5 degrees.
3
3
J Releasing the Arm Lock

Releasing the arm lock enables rotation, extension/contraction, and up/down movements of the arm.
In addition, radiography parameters are displayed on the X-ray control panel and radiography is
enabled. In this state, the system will be in the low-speed travel mode, where maximum travel speed
is limited to about half of the normal travel speed.
The lock can be released in one of the following three ways:
Lift up the X-ray tube unit while pressing the arm lock release button on the collimator
control handle.
Lift up the X-ray tube unit while holding down the arm lock release lever located at the arm
joint section.
Lift the arm while pressing the arm lock release button located at the guide handle grip.
3
3
3
3
3
M503-E027
3-13
3 Basic Operation
Arm Lock
Release
Lever
Arm Lock
Release
Button
View From A
Arm Lock
Release
Button
J Setting the Arm Lock

Once the arm is locked, the system enters the normal travel mode and maximum speed is about
5 km/h.
Arm Lock
Release Button
Locking Pin
Locking Pin
Hole
3-14
Push the X-ray tube unit as far as possible toward the column until it
makes contact with the stopper, while pressing the arm lock release
button.
2
3
Return the tilt of the X-ray tube unit and collimator to the center position.
Insert the locking pin, located on the lower surface of the arm, into the
locking pin hole in the arm joint section.
Slowly push the X-ray tube unit down while pressing the arm lock release
button.
M503-E027
3.4 Arm Operation
After locking the arm, a sound is emitted and the status indicator lamp
switches OFF.
3
3
When lowering the X-ray tube unit, ensure that the front of the
collimator does not hit the control panel buttons or the panel itself.
Do NOT place your hand on the column cover.

By doing so, a part will protrude from a hole in the cover when the arm
moves up and down.
3.4.2
3
3
Positioning the X-Ray Tube Unit
3
Do NOT rotate the X-ray tube unit more than 180 degrees around the
arm axis.
Doing so may damage the cables.

The rotated and tilted position of the X-ray tube unit is held by frictional force (no button operations
are needed to change the tilt of the X-ray tube unit).
When positioning the X-ray tube unit, use the angle indicator label as a reference for rotating
the unit around the arm axis.
3
3
Angle Markings
Pointer
X-ray Tube Unit
3
3
3
M503-E027
3-15
3 Basic Operation
Use the angle indicator label as a reference for rotating the X-ray tube unit around the tube
axis. Turn the knob to secure it in place or release it.
X-ray Tube Unit
Angle Markings
Pointer
Knob
3-16
Click stops are provided every 90 degrees as a tactile guide for positioning the X-ray tube unit
exactly both vertically and horizontally.
M503-E027
3.4 Arm Operation
3.4.3
Setting the Irradiation Field
J Adjusting the Irradiation Field

When setting the X-ray irradiation field, operate the irradiation field adjusting knobs on the front of
the collimator. Adjust the size of the irradiation field by referring to the following two guides:
The tape measure attached to the side of the collimator
The angle markings printed on the front of the collimator
3
3
3
Angle Markings
Tape Measure
3
3
Irradiation Field Adjusting Knob
In addition, loosening the knob on the top of the collimator allows the collimator to be rotated around
the X-ray axis.
3
3
Knob
3
3
3
3
3
M503-E027
3-17
3 Basic Operation
J Irradiation Field Reference Light

Illuminating this light allows confirming the X-ray irradiation field.
The cross-hair intersection in the light field indicates the center of the X-ray irradiation field.
The collimator lamp buttons are located on the front of the collimator, the X-ray control panel, and
remote control (optional). Pressing any of these buttons switches on the collimator lamp. The
collimator lamp is automatically turned off after about 30 seconds. It is also turned off by pressing
the button once more.
* The collimator lamp can also be turned ON or OFF by pressing the radiography hand switch to the first
level and then immediately releasing it.
If radiography preparation is performed while the collimator lamp is illuminated, the

collimator lamp turns OFF. When radiography preparation is finished, the collimator
lamp turns ON again.
^ Reference If the collimator lamp does not turn ON again even after radiography preparation is
finished, see "4.1 User Settings" P.4-2.
3-18
M503-E027
3.5 Setting the Radiography Parameters
3.5
3.5.1
Setting the Radiography Parameters
Radiography parameters on this system are set using two controls X-ray tube voltage and currenttime product. Based on the radiography tube current-time product (mAs) setting, the system
automatically determines the maximum X-ray tube current (mA) and the shortest exposure time(s)
available within the rated limits of the system and X-ray tube unit. Radiography parameters can be
changed using the methods described below.
The radiography parameter settings permitted on the MobileArt Evolution High Power Type (32
kW) are constrained by X-ray tube voltage (kV), current-time product, and radiography mode.
^ Reference For more details regarding radiography parameter settings,
3
3
See "8.2 Specifications" P.8-8.
3.5.2
Setting the Radiography Parameters Using the Anatomical
Programs (APR)
J Selecting an Anatomical Program for Cassette Radiography Mode

Use the X-ray control panel buttons to select the registered radiography parameters. The LED light
for selected buttons will be illuminated.
Button
Select the imaging region.

Imaging
Region
Button
Imaging
Region
Button
Imaging
Region
Head
Waist
Arm
Chest
Leg
Hand
Abdomen
Foot
3
3
Select the projection direction.

Button
Projection
Direction
Front
Button
Projection
Direction
Button
Lateral
Projection
Direction
3
3
Oblique
3
3
M503-E027
3-19
3 Basic Operation
Select the body thickness correction setting.
Button
Body
Thickness
Button
Thin
Body
Thickness
Body
Thickness
Button
Normal
Thick
Examples of selecting anatomical programs

Example of frontal projection of the abdomen of a patient with a standard body type.
3.5.3
Select the imaging region: Press the
Select the projection direction: Press the
Select body thickness correction: Press the
(abdomen).
(frontal projection).
(normal).
Manually Setting the Radiography Parameters

When manually setting the radiography parameters, refer to the methods described
below.
If settings registered in the anatomical program are changed, the imaging region,
projection direction, and body thickness correction selection buttons will blink.
J Setting the X-ray Tube Voltage (kV)

The setting value is shown on the kV display.
Press the [+] button to increase X-ray tube voltage setting in 1 kV increments.
Press the [-] button to decrease X-ray tube voltage setting in 1 kV decrements.
Hold down the [+] or [-] button to change the setting more quickly.
J Setting the Current-Time Product (mAs)

The set value is shown on the mAs display.
Press the [+] button to increase the product in 1-step increments.
Press the [-] button to decrease the product in 1-step decrements.
Hold down the [+] or [-] button to change the setting more quickly.
J Changing the Focal Spot

Use the
3-20
(focus mode button) to change between large and small focuses.
When LED is not illuminated, a large focus is selected.
When LED is illuminated, a small focus is selected.
M503-E027
3.6 X-Ray Radiography
3.6
X-Ray Radiography
X-ray tube units must be aged before they can be used. Always age the X-ray
tube unit before radiography.
Inadequate aging may result in the X-ray tube unit discharging during
radiography.
Release the arm lock during radiography.

Radiography is not possible when the system is being moved. To perform
radiography, release the grip bar and inch-mover buttons.
Using the collimator, adjust the X-ray irradiation field to the required range, and
then start radiography.
3
3
^ Reference "3.4.3 Setting the Irradiation Field" P.3-17
3
3
3
3
3
3
3
M503-E027
3-21
3 Basic Operation
3.6.1
Cassette Radiography Procedure
Select an anatomical program from the X-ray control panel, or set

radiography parameters from the current-time product and tube voltage
buttons.
Press the hand switch button to the first level (radiography preparation).
Radiography preparation begins and the status indicator lamp will blink green.
* If the
(standby indicator lamp) is not illuminated, radiography preparation cannot start.

Before pressing the hand switch, confirm that the indicator is illuminated.
During radiography preparation, the collimator lamp will turn OFF automatically.
Pressing the Hand Switch

to the First Level
After radiography preparation has finished, the

(radiography ready indicator lamp)
will be illuminated and the status indicator lamp is illuminated green and the collimator
lamp is illuminated again.
* If an X-ray is not radiated within 30 seconds after the radiography preparation is finished,
the preparation will be automatically cancelled. To prepare for radiography again, release
the hand switch from the state pressed to the first level.
To prevent the collimator lamp from turning ON again after the radiography preparation is
finished, see "4.1 User Settings" P.4-2.
3-22
M503-E027
When the
(radiography ready indicator lamp) is illuminated, press the
hand switch button to the second level (X-ray exposure).
Pressing the button starts X-ray exposure.
During X-ray exposure, the
(X-ray irradiation indicator lamp) is illuminated, a sound
is emitted, and the status indicator lamp will be illuminated orange.
* The sound volume during X-ray exposure can be made louder.
3
3
3
to the Second Level
3
3
3
After X-ray exposure, the [kV] and [mAs] displays will blink for 5 seconds.
The status indicator lamp will blink until the battery has recharged.
* After performing radiography, another image cannot be taken until the battery is recharged.
Wait until the
(standby indicator lamp) is illuminated before performing any operation.
Depending on the radiography parameters, this may require 1 minute or more.
During radiography the hand switch (first and second levels) must be continuously and fully
depressed until the exposure finishes. If the switch is released before completion of the
exposure, the exposure will be terminated prematurely. In this case, the film may not be
clear due to insufficient X-ray exposure.
When repeating radiography preparation, release the hand switch (first and second levels)
once.
3
3
3
3
3
3
3
M503-E027
3-23
3 Basic Operation
3.6.2
Low-Battery Radiography
If the battery indicator indicates status 3; shown in the table below, the battery must be charged. But
if the battery indicator indicates status 2, radiography is still possible in the low-battery mode,
within the restrictions indicated below.
No.
Battery Indicator
X-ray Radiography Availability

Radiography is possible.
Low Battery only low-battery radiography is possible.
2
Blinking
^ Reference "3.6.2 Low-Battery Radiography" P.3-24
Radiography is not possible.

3
J Current-Time Product Limits for Low Battery Voltage

Low-battery radiography limits DR radiography parameters and exposure may take longer than
normal.
^ Reference "8.2.3 High-Voltage Generator" P.8-9
3-24
M503-E027
3.6.3
Additional Radiography Function
If the system is used continuously while the battery is low, radiography will not be possible.
After the battery indicator stops blinking, if additional radiography is needed, about ten more times is
possible (when radiography condition is general chest radiography).
1
2
Turn the key switch OFF
Turn the key switch ON

button).
in combination with the
When the LED is blinking on the battery indicator
(user settings
3
3
, low-battery radiography is
possible.
Charge the battery as soon as possible if the necessary radiography is finished.
The number of the possible radiography depends on the battery condition.
Radiography will not be possible when the battery is depleted.
3
3
3
3
3
3
3
3
3
M503-E027
3-25
3 Basic Operation
3.7
Charging the Battery
Charge the battery in a well-ventilated room.+

Do NOT cover the system during the charging of the battery.
When pulling out the power cable, hold the plug portion and do NOT
apply excessive force to the cable.
Excessive force may damage the cable or internal cable reel.
When rewinding the cable, hold the plug until it is completely
retracted.
3-26
Charge the battery under the environmental conditions specified in "1.3

Environmental Conditions" P.1-4. Charging the battery under conditions
exceeding these limits may significantly reduce battery life and overall
performance.
Attach an additional protective ground wire with maximum 100 ground

resistance, during the charging of the battery.
To maximize battery life and performance, recharge the battery after one or more
LEDs on the battery indicator go off. Charging a fully charged battery may have an
adverse affect on battery life and performance.
System travel (movement) is not possible while the power cable is connected to a
power outlet.
Radiography is not possible while charging.

When the key switch is set to ON
, charging stops and X-ray radiography can
be performed.
M503-E027
3.7 Charging the Battery
J Charging After Installation

To stabilize battery performance, it is recommended that, after installation, the system is used until
no battery indicator LEDs remain illuminated before recharging. Repeat this cycle several times.
J Charging Procedure
1
2
Turn ON the main circuit breaker.

Turn the key switch OFF
Recharging is not possible with the key switch ON.
When turning the key switch ON during the charging of the battery, wait more than
2 seconds until turning the key switch OFF again.
Pull the power plug out from the front of the system and insert it into a
power outlet.
3
3
3
Power Plug
3
The
(power line connection indicator lamp) is illuminated. After about 10 seconds
the battery begins charging. During charging, the
(charging lamp) is illuminated
and the battery indicator indicates the charging status.
Charging
Lamp
Battery Indicator
Blinking
3
3
Charging Status
Charging in progress.
indicates battery is at
least 90% charged.
Illuminated
Fully charged.
3
Indicator segment is illuminated if shown in black J and off if shown in white F above.
3
M503-E027
3-27
3 Basic Operation
When the battery is fully charged, charging automatically stops and the
(charging
lamp) is illuminated. It normally takes approximately five hours to charge a battery from
no indication on the Battery Indicator to charged, to a level of 90%, (the Battery Indicator
being fully illuminated). When the battery is charged for more than eight hours it is at
100% capacity (10 hours max.).
When turning ON the key switch, the
During charging, the battery indicator shows the charging status, not the amount
charged.
Please note that the battery voltage rises temporarily immediately after charging.
As a result, the battery indicator will indicate more than the actual remaining
charge. After the system is used for a short period, the battery display will display
the actual remaining charge.
If charging is interrupted, the battery indicator will initially be lit up completely.
After a short period, the number of lights may decrease suddenly, but this does
not indicate a malfunction.
Charging will take a long time if performed with the DR system operating. When
charging the battery, stop the DR system after its operation is finished (only with
FPD upgrade).
3-28
(charging lamp) will turn OFF.
After charging, unplug and stow the power cable.
M503-E027
Chapter
Advanced Operation
J Chapter Contents
4.1
User Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-2
4.2
Changing the Operation Sound Volume . . . . . . . . . . .4-12
4.3
Changing Anatomical Program Parameters . . . . . . . .4-14
4.4
Releasing the Brake in Emergency . . . . . . . . . . . . . . .4-17
4.5
Notification Function . . . . . . . . . . . . . . . . . . . . . . . . . .4-18
4 Advanced Operation
4.1
User Settings
Item
kV Display
Description
Ref.
Personal ID Setting
Sets and changes personal ID numbers.
P.4-4
Power-Assist Setting
Adjusts the operational characteristics of moving the

system.
P.4-4
Acceleration Setting
Adjusts the acceleration characteristics.
P.4-5
Steer Control Setting
Adjusts the turning characteristics.
P.4-5
Backward PowerAssist Setting
Adjusts the backing characteristics.
P.4-6
Auto-Power-Off Time
Setting
Changes the setting time of the auto-power-off function.
P.4-6
Sets volume of sound emitted from control panel buttons.

Buzzer Setting
Collimator Lamp
Control Setting
P.4-7
Sets volume of warning sound emitted when obstruction

detector is activated.
Enables or disables using hand switch to control radiation
field reference light.
Specifies radiation field reference light after radiography
preparation is finished.
P.4-7
APR Settings at
Startup
Specifies APR radiography parameters specified at startup.
P.4-8
Operation Sound
Setting
Sets the sound tone and volume of the sound emitted

during X-ray exposure or system travel, or when
radiography preparation is finished.
P.4-9
The grade ability changes in accordance with user settings data (PAS, Acc,
and bAc) for the characteristics of moving the system. The grade ability
decreases when a set value is small. The grade ability increases when a set
value is large.
4-2
M503-E027
4.1 User Settings
4.1.1
Entering the User Settings Mode
After holding down the

(user settings button) for about 1 second, [usr ope] appears on the Xray control panel momentarily and the display returns to the user settings mode.
After changing to the user settings mode, [Pid] first appears on the kV display.
Toggle through the setting items by pressing kV [+] and kV [-] buttons.
Normal Mode
Press the
(user settings button) for
about 1 second.
Press the
or
Press the
(registration button).
(user settings button).
User Settings Mode
Press the kV [-] button.
4
4
Press the kV [+] button.
4
4
4
If keyless entry is set, after changing to the user settings mode, [PAS] first
appears on the display. [Pid] does not appear on the display.
J Registering Changed Data

Press the
This saves the changes to data, displays [rec ord] on the X-ray control panel, and returns to the
normal mode.
J Not Registering Changed Data

Press the
(user settings button).
This returns to the normal mode without saving changes.
* It is possible to register changed data for multiple items at once.

M503-E027
4
4-3
4.1.2
Personal ID Setting [Pid]

Personal ID number is displayed on the mAs display.
The personal ID number can be set using any 10 digits, from 0 to 9.
Press the mAs [+] and mAs [-] buttons to change personal ID number.
Other settings can be registered for each personal ID.
4.1.3
Power-Assist Setting [PAS]

The power-assist setting is displayed on the mAs display.
Press the mAs [+] and mAs [-] buttons to change the setting.
mAs Display
Level of Power Assist
100
Easier to Move
95
75
70
Normal
65
35
30
Harder to Move
Power-assist is set to [70] when delivered.

If nothing else needs setting, press the
(registration button) to register the settings. [rec ord]
appears on the X-ray control panel and the user settings mode returns to normal mode.
4-4
M503-E027
4.1 User Settings
4.1.4
Acceleration Setting [Acc]
The acceleration setting is displayed on the mAs display.

mAs Display
Level of Acceleration Setting
100
Accelerates more quickly
95
65
60
Normal
55
35
30
Accelerates more slowly
4
4
4
4
4
Acceleration is set to 60 when delivered.

4
4.1.5
Steer Control Setting [stc]
The steering setting is displayed on the mAs display.

mAs Display
Effect on Steering
100
Easier to turn (normal)
95
90
55
50
Easier to go straight
4
4
4
4
Steering control is set to [100] when delivered.

4
M503-E027
4-5
4.1.6
Backward Power-Assist Setting [bAC]

The backward power-assist setting is displayed on the mAs display.
mAs Display
Level of Power-Assist for Backward Movement
100
Easier to move backward
95
85
80
Normal
75
55
50
Harder to move backward
Backward power-assist is set to [80] when delivered.

4.1.7
Auto-Power-Off Time Setting [APO]

The auto-power-off setting is displayed on the mAs display.
mAs Display
Auto-Power-Off Delay
--
Auto-power-off not set
05
5 minutes
10
10 minutes
15
15 minutes (normal)
20
20 minutes
30
30 minutes
Auto-power-off is set to 15 minutes when delivered.

* The auto-power-off function does not turn the DR system OFF (only with FPD upgrade).
See "3.1.2 Shutting Down the System" P.3-4.
4-6
M503-E027
4.1 User Settings
4.1.8
Buzzer Setting [bon]
The sound setting is displayed on the mAs display.

mAs Display
Sound Setting
A sound is emitted when X-ray control panel buttons are pressed.
A sound is emitted if the obstruction detector is activated (unless the
obstruction detection feature is cancelled).
No sound is emitted when kV [+], [-] or mA [+], [-] buttons are held
down to change radiography parameters rapidly.
No sound is emitted when the obstruction detector is activated.
No sound is emitted when buttons on the X-ray control panel are
pressed (except when registering anatomical programs or changing
settings).
4
4
No sound is emitted when the obstruction detector is activated.
Sound is set to [on] when delivered.

4.1.9
Collimator Lamp Control Setting [LAP]
Collimator lamp control setting is displayed on the mAs display.

Press the mA [+] and mA [-] buttons to change settings in the follow sequence:
[O-C][N-N][E-N][O-N][N-C][E-C][O-C]
Left Side of mAs Display
Collimator Lamp Setting
After radiography preparation is finished, the collimator lamp is

illuminated until X-ray exposure starts, or for up to approximately 10
seconds, regardless of whether the collimator lamp is turned ON or
OFF when the radiography preparation starts.
The collimator lamp turns OFF during radiography preparation (stop

radiography preparation to turn ON the collimator lamp).
If the collimator lamp is ON, it turns OFF when radiography
preparation starts, then turns back ON after preparation is finished and
remains ON until X-ray exposure starts, or up to a maximum of about
10 seconds.
Right Side of mAs Display
Collimator Lamp Setting
4
4
Enables using the hand switch to turn the collimator lamp ON/OFF.
Disables using the hand switch to turn the collimator lamp ON/OFF.
Collimator lamp control is set to [ O - C ] when delivered.

M503-E027
4-7
4.1.10 APR Settings at Startup [aPr]

The APR startup setting is displayed on the mAs display.
mAs Display
APR Settings at Startup
Remembers and restores radiography parameters from just before the

power was shut OFF (if APR radiography parameters were changed
manually, the changed parameters are restored).
Restores the parameters for the APR that was used just before the
power was shut OFF (if APR radiography parameters were changed
manually, parameters registered for that APR are restored, rather than
the changed parameters).
Displays the parameters for the preselected APR. Select the APR
buttons to display at system startup on the X-ray control panel
(imaging region, projection direction, and body thickness correction).
The corresponding LEDs illuminate. The APR parameters specified
are displayed at system startup.
The APR startup setting is set to [ 0 ] when delivered.

4-8
M503-E027
4.1 User Settings
4.1.11 Operation Sound Setting [Snd]
On the X-ray control panel, the 3rd digit of the mAs display displays the sound pattern setting No.
The 2nd digit shows the sound tone No. and the 1st digit shows the volume value.
mAs display, 3rd digit (sound pattern)

mAs display, 2nd digit (sound tone)
mAs display, 1st digit (sound volume)
Operation Sound Volume
Settings
4
4
4
Pattern Selection
Registration
System Travel Alert Sound

Setting at Power-Up
Operation Sound Pattern

Tone Settings
Checking the Operation Sound
Pattern Tone and Volume
4
4
J Pattern Selection
Use the mAs [-] switch to select the sound pattern setting No.
3rd Digit in mAs Display
(Operation Sound Number)
Pattern
The sound emitted during X-ray exposure.
The sound emitted when radiography preparation is finished.
The sound emitted during system travel to alert people of approaching

mobile unit.
4
4
J Setting the Pattern Tone

Use the mAs [+] button to set the tone of the sound pattern.
Select from 7 sound tones.
4
4
M503-E027
4-9
J Setting the Sound Volume

Set the sound volume.
The
(sound volume) setting shown by the 1st digit of the mAs display increases each time the
sound button is pressed.
1st Digit in mAs Display
(Volume Setting Number)
Sound Volume Setting
No sound (during X-ray exposure a minimum level of operation

sound is emitted)
Minimum volume
Normal
High
Sound volume is set to "4" when shipped.
Even if the X-ray exposure sound is set to mute, a minimum level of sound is still
emitted to warn those in the vicinity that X-ray radiation is present.
J Setting the sound emitted during X-ray exposure.
4-10
Press the mAs [-] button until "1" is displayed in the third digit of the mAs
display.
2
3
4
Press the mAs [+] button to set the sound tone.

Press the
(sound button) to set the sound volume.
Press the
(registration button) to register the settings.
[rec ord] appears on the X-ray control panel and the user settings mode
returns to normal mode.
M503-E027
4.1 User Settings
J Setting the sound emitted when radiography preparation is finished.
display.
2
3
4

Press the
Press the
4
4
J Setting the sound emitted during system travel
display.
2
3
4

Press the
Press the
(remote controller button) and determine whether or not to
emit a system travel alert sound for the setting at power-up.
When the remote controller button is illuminated, holding the brake release
lever will emit a system travel alert sound.
4
4
4
* When the remote control button is not illuminated and the 1st digit of the mAs display is
blinking, no system travel alert sound will be emitted if you hold the brake release lever.
To turn the system travel alert sound ON or OFF temporarily without changing the operation
sound setting, lock the arm and hold down the collimator lamp button 1 second or longer.
See"4.2 Changing the Operation Sound Volume" P.4-12
Press the
4
4
4
4
When the system is turned OFF, the system travel alert sound ON/OFF will return to
that made at the operation sound setting [Snd].
4
J Checking the Sound Pattern
Press the collimator lamp button on the X-ray control panel to confirm the sound tone and volume.
M503-E027
4-11
4.2
Changing the Operation Sound Volume

The operation sound volume can be easily changed by operating the sound button on the X-ray
control panel or the collimator lamp button.
J Changing the Sound Volume Emitted During X-Ray Exposure or When

Radiography Preparation Is Finished
Press the sound button on the X-ray control panel to change the sound volume emitted during X-ray
exposure or when radiography preparation is finished, as shown below.
Sound volume set at the operation

sound setting [Snd]
(LED on the sound button illuminates)
Minimum Volume
(LED on the sound button blinks)
Mute
(LED on the sound button is OFF)
Even if the X-ray exposure operation sound is set to mute, a minimum level of
operation sound is still emitted to warn those in the vicinity that X-rays radiation is
present.
When the system is turned OFF, the operation sound volume will be reset to that
made at the operation sound setting [Snd].
^ Reference "4.1.11 Operation Sound Setting [Snd]" P.4-9
4-12
M503-E027
4.2 Changing the Operation Sound Volume
J Using the Collimator Lamp Button to Adjust Volume

When the collimator lamp button is held down 1 second or longer with the arm locked, the system
travel alert sound will be turned ON or OFF as shown below.
4
4
Sound volume set at the operation

sound setting [Snd]
4
Mute
4
4
If the operation sound volume is set using the sound button on the X-ray control
panel or the collimator lamp button, the system travel alert sound volume will be reset
to that made at the operation sound setting [Snd] when the system is turned OFF.
^ Reference "4.1.11 Operation Sound Setting [Snd]" P.4-9
4
4
4
4
4
4
4
M503-E027
4-13
4.3
4.3.1
Changing Anatomical Program Parameters

Registering Anatomical Programs
In the anatomical program, a total of 72 types (8 imaging portions x 3 directions x 3 body
thicknesses) are possible.
The following radiography parameters can be registered in the anatomical programs.
X-ray tube voltage, X-ray current-time product and focal spot size
^ Reference "2.4 X-Ray Control Panel" P.2-6
J Registration Procedure for Cassette Radiography
Select the anatomical program to be registered for cassette radiography

mode.
Select the imaging region, projection direction, and body thickness correction.
Specify the radiography parameters and focus size to be registered.

Make sure that the imaging region, projection direction, body thickness correction,
radiography parameters, and focal spot size are specified as intended.
Press the
(registration button) for about 3 seconds.
A sound is emitted and the
(registration button) blinks.
Keep pressing the

(registration button) until [aPr set] appears on the X-ray control
panel, which indicates the anatomical program has been registered.
When registering anatomical programs, do not release the registration button until
[aPr set] appears on the X-ray control panel.
4-14
M503-E027
4.3 Changing Anatomical Program Parameters
4.3.2
Deleting Unused Anatomical Programs
Anatomical programs not normally used, can be deleted.

Once an anatomical program is deleted it can no longer be used for radiography, even if it is selected.
If a deleted anatomical program is selected, [aPr set] appears on the X-ray control panel.
J Deleting Unused Anatomical Programs
Select the anatomical program to delete.

Select the unused imaging region, projection direction, and body thickness correction.
Hold down the

about 3 seconds.
(registration button) and press mAs [+] button for
Keep pressing the

(registration button) and mAs [+] button until [del ete] appears on
the X-ray control panel, which indicates the anatomical program has been deleted.
[_ _ _ _ _ _] appears on the X-ray control panel.
4
4
4
4
4
4
4
4
M503-E027
4-15
J How to Use the Deleted Anatomical Program

If a deleted anatomical program is selected, [_ _ _ _ _ _] will appear on the X-ray control panel and
radiography is not possible.
However, the following procedure allows using a deleted anatomical program temporarily.
Select the deleted anatomical program.

Select the deleted anatomical program to be used. [_ _ _ _ _ _] appears on the X-ray
control panel.
Hold down kV [+] or kV [-] button, or mAs [+] or mAs [-] button for about 3
seconds.
A sound is emitted.
Continue pressing the button until [_ _ _ _ _ _] disappears from the X-ray control panel
and radiography parameters are displayed.
Radiography parameters in the X-ray control panel will be displayed and allow the use of
the deleted anatomical program for radiography.
4-16
To enable using a deleted anatomical program, keep holding down kV [+] or kV [-]
button, or mAs [+] or mAs [-] button until the radiography parameters appear on
the X-ray control panel.
This procedure only temporarily enables the use of deleted anatomical program.
To register the radiography parameters used, register them as an anatomical
program.
M503-E027
4.4 Releasing the Brake in Emergency
4.4
Releasing the Brake in Emergency

This system is equipped with a function to release the brake in an emergency, such as a case when
the system malfunctions or the battery runs out.
4
4
Only use the brake release function in emergencies.
Be especially careful when using the brake release function on

sloped surfaces.
4.4.1
Activating the Brake Release Function
1
2
Turn OFF
the key switch on the power supply panel.
Press the emergency stop button.

This activates the brake release function.
* When the brake release function is activated, the brake release lever on the grip bar does not
function. The key switch is also turned OFF, so power-assist does not function either.
4.4.2
Releasing the Brake in Emergencies
4
4
While pressing the emergency brake release button located to the left of
the grip bar, the brake is released to allow moving the system by hand.
Emergency Brake Release Button
4
4
4
4
M503-E027
4-17
4.5
Notification Function
To maintain the system performance, some parts must be replaced periodically.
The system is equipped with a function to notify users of the replacement period for some parts.
If it is time to replace a part of the X-ray control panel will display the warning and replacement time
when the key switch is turned ON
.
The kV display indicates the part code for the replacement part and the mAs display indicates the
number of cycles before reaching the replacement date.
kV Display
Part
Information on Replacement Time Display
U01
Battery
Displayed after 2 years from installation.
U02
CPU Backup Battery
U03
Emergency Brake
Release Battery
U04
X-Ray Tube Unit
Displayed after 30,000 exposures from installation.
U05
Motor
Displayed after the system travels 7,500 km from installation.
The registration button blinks while the replacement time is displayed.

Press the blinking registration button to cancel the replacement time and warning indicator lamp and
return to normal operating mode.
When a replacement time and warning indicator are being displayed, all operations
except brake release and arm operations are disabled.
4-18
M503-E027
4.5 Notification Function
J Confirming the Usage Period, Count and Distance Information for Each
Part
Turn the key switch to ON
while holding the remote control button down, to display the usage
period, count, and distance information for each part in the kV and mAs displays on the X-ray
control panel.
Toggle between information for each part by pressing the kV [+] and [-] buttons, or the imaging
region selection buttons, to display the information. This causes the lamp to blink for the region
button corresponding to the selected replacement part.
4
4
4
4
4
Remote Control Button
Imaging Region
Selection
Button
Part
Information Displayed in kV and mAs Displays
4
Battery
Number of months used
CPU Backup Battery
Emergency Brake
Release Battery
X-Ray Tube Unit
Times X-rays were exposed
Motor
Distance traveled
4
4
4
When the part information and warning indicator are blinking in the kV and mAs displays, it
indicates it is time to replace the corresponding part.
To return to the normal operating mode, temporarily switch the power OFF and restart the system.
4
4
When the part information and warning indicator are being displayed, all operations
except brake release and arm operations are disabled.
M503-E027
4-19
J Temporarily Disabling the Replacement Time Display Function

Use the following procedure to temporarily disable the replacement time display function.
Turn the key switch ON while pressing the remote controller button on the
X-ray control panel. Check the data on usage, number of cycles, and
distance for each part.
Press the mAs [+] and [-] buttons.

This displays [clr] [ no] in the kV and mAs displays on the X-ray control panel.
Press the mAs [+] and [-] buttons.

This displays [clr] [yes] in the kV and mAs displays on the X-ray control panel.
With [clr] [yes] shown on the kV and mAs displays, hold the registration
button down for at least 3 seconds.
This can temporarily disable the replacement time display function.
Even if the replacement time display function is temporarily disabled, after a given period of time
has elapsed, a warning sound is emitted and a replacement time and warning indicator are displayed
on the X-ray control panel when the key switch is turned ON .
The period for which the replacement time display function can be temporarily disabled differs
depending on the part.
Part
4-20
Period Notification Function Can Be Temporarily Disabled
Battery
1 month
CPU Backup Battery
1 month
M503-E027
4.5 Notification Function
Part
Period Notification Function Can Be Temporarily Disabled
Emergency Brake Release Battery
1 month
X-Ray Tube Unit
3000 exposures
Motor
100 km travel distance
4
4
4
While the replacement time display function is temporarily disabled, the above
cancellation procedure cannot be performed until the replacement time display
function is enabled again.
4
4
4
4
4
4
4
4
4
4
M503-E027
4-21
Chapter
Optional Features
J Chapter Contents
5.1
Remote Controller . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-2
5.2
Protective Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-5
5.3
Dose Area Product Meter . . . . . . . . . . . . . . . . . . . . . . .5-7
5.4
Dose Calculation Unit . . . . . . . . . . . . . . . . . . . . . . . . . .5-9
5.5
Distance Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
5.6
Keyless Entry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-12
5.7
Changing the Grip Bar Height . . . . . . . . . . . . . . . . . . .5-14
5.8
Luminous Hand Switch . . . . . . . . . . . . . . . . . . . . . . . .5-15
5.9
Additional Hand Switch . . . . . . . . . . . . . . . . . . . . . . . .5-16
5.10 Grid Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-17

5.11 Large Cassette Box . . . . . . . . . . . . . . . . . . . . . . . . . .5-18
5.12 FPD Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-19
5 Optional Features
5.1
Remote Controller
Using the infrared remote controller allows performing radiography and switching the collimator
lamp ON or OFF remotely.
Make sure no TV or other remote controllers are being operated in the room before
using the remote controller for radiography.
Make sure the remote control receiver is not exposed to bright lights, such as
incandescent lamps.
4
1
2
3
No.
5-2
Name
Function
Radiography Preparation
Button
Starts radiography preparation.
X-ray Exposure Button
Starts X-ray exposure when pressed in combination with the

radiography preparation button.
Collimator Lamp Button
Turns collimator lamp ON/OFF.
Transmission Status
Indicator
A red LED is illuminated when the remote controller is transmitting a

command to the main unit.
M503-E027
5.1 Remote Controller
J Using the Remote Controller
5
5
If the red LED transmission status indicator is illuminated even if no

remote controller button is pressed, this indicates a fault with the
remote controller. Stop using the remote controller, remove the battery,
and contact your Shimadzu service representative.
Press the
(remote controller button) on the X-ray control panel to
illuminate the LED.
Press the radiography preparation button while aiming the remote

controller at the remote control receiver.
The system status indicator lamp will blink green.

^ Reference "Infrared Remote Control Receiver" P.5-4
Keep pressing the radiography preparation button until the

(radiography ready indicator lamp) is illuminated on the X-ray control
panel.
When the
is finished.
(radiography ready indicator lamp) is illuminated, radiography preparation
The system status indicator lamp is illuminated green.
* If using the DR system for radiography, confirm the DR system READY indicator before
attempting radiography. Attempting radiography before the DR system is ready will result in
error F68 and prevent radiography.
Press the X-ray exposure button while pressing the radiography

preparation button.
This irradiates the subject with X-rays and the system status indicator lamp is illuminated
orange.
Once the X-ray exposure using the remote controller has finished, the remote controller is
disabled for safety reasons and the LED of the
(remote controller button) is turned
OFF.
To continue using the remote controller for radiography, press the
controller button) so the LED is illuminated.
5
5
(remote
* When the
(remote controller button) is illuminated, using the hand switch for

radiography will turn OFF the LED and disable the remote controller.
Once radiography preparation starts, keep aiming the remote controller transmitter at the
receiver until the X-ray exposure is finished.
5
5
M503-E027
5-3
5 Optional Features
J Operable Range of the Remote Controller

The remote controller is operable within a radius of 5 meters and range of 270 degrees around the
remote control receiver.
Operable Range of the Remote Controller
Infrared Remote
Control Receiver
5m
270
Infrared Remote Control Receiver
Receiver
Arm Joint
The operable range of the remote controller may be affected by surrounding

conditions.
J Replacing Batteries
If the remote controller transmission status indicator is not illuminated when pressing the remote
controller button, replace the batteries.
5-4
Slide the battery cover on the back of the remote controller in the direction
of the arrow, and remove the cover.
2
3
Exchange the old batteries with new AA batteries (2 cells).

Re-install the battery cover on the remote controller.
M503-E027
5.2 Protective Screen
5.2
Protective Screen
Operator exposure can be reduced by using the protective screen.
5
Item
Specification
Lead Impregnated Acrylic
Lead equivalent min. 0.3 mm Pb
Dimensions (during usage)
W46 cm H34 cm 0.8 cm thick
J Using the Shield
Before radiography, stand the protective screen in place by pulling the

handle toward yourself.
Handle
5
5
2
After radiography, fold the protective screen down by pulling on the

handle.
Handle
5
5
5
5
M503-E027
5-5
5 Optional Features
5-6
Do not rotate the column, raise/lower or store the arm with the protective screen in
the standing position.
Doing so could cause the arm or column to hit and damage the screen.
Handle the protective screen carefully.

Accidentally tipping the protective screen over may damage it.
Do not move the system with the protective screen left in the standing position.
Tipping the screen over could damage the screen, cover, or other parts.
Be sure to store the protective screen in the folded position.

Storing the screen unfolded may cause the arm to hit the collimator when stowing
the arm.
Using the protective screen limits the optional remote controller's operating range.
M503-E027
5.3 Dose Area Product Meter
5.3
Dose Area Product Meter

The dose area product meter is attached to the front of the collimator and displays the dose-area
product on the dose-area display.
After turning the power ON, wait 3 minutes for the dose area product meter to stabilize.
5
5
5
Display Unit
5
5
Do NOT subject the dose area product meter to mechanical forces.

Doing so could damage or break the dose area product meter.
5
5
The dose area product meter cannot be attached concurrently with "5.4 Dose
Calculation Unit" P.5-9 or "5.5 Distance Indicator" P.5-11.
5
J Using the Dose Area Product Meter
1
2
3
4
Position the X-ray tube unit at the imaging position.
Perform exposure.
Confirm the dose-area product indicated on the dose area product meter.
The display is reset if radiography parameters change or radiography

preparation starts.
5
M503-E027
5-7
5 Optional Features
J Cleaning the Dose Area Product Meter

To clean the dose area product meter, wipe the surface with cloth soaked in pH-neutral cleaner and
which is thoroughly wrung out.
Do NOT pour water on the dose area product meter or use cleaning
agents containing solvents (such as benzene or alcohol) or organic
solvents.
Doing so could break or damage the meter.
5-8
Make sure no moisture enters the dose area product meter during cleaning. After
cleaning, dry it thoroughly before use. Clean the buttons by wiping it with a cloth
soaked in a disinfectant.
After the FPD upgrade, the dose-area product is displayed on the DR system and
the dose-area display, and is recorded in the DICOM image header.
Units of dose-area product are "mGy cm2" on the display and "dGy cm2" in
the DICOM image header.
M503-E027
5.4 Dose Calculation Unit
5.4
Dose Calculation Unit
The dose calculation unit calculates and displays the X-ray radiation dosage applied to the surface of
the patients skin during radiography. The calculation is based on the radiography parameter settings
and the distance between the surface of the patient and X-ray tube unit focal spot which is measured
by an ultrasonic ranging unit attached to the collimator.
5
5
5
5
Display Unit
Calculation Method/
Dose (mGy) =
C (kV) mAs 1
(focal spot - patient surface distance)2
C (kV): Correction factor of X-ray tube voltage
C (kV) depends on factors such as radiation quality and system used and is calibrated during
installation.
mAs: Current-time product
J Using the Dose Calculation Unit
Position the X-ray tube unit and specify the radiography parameters in the
same manner as normal X-ray radiography.
Based on the radiography parameter settings and the distance between the surface of the
patients skin and the X-ray tube unit focal spot, the dose calculation unit calculates and
displays the X-ray radiation dosage given to the patient during radiography.
5
5
5
5
5
M503-E027
5-9
5 Optional Features
The calculated values displayed by this dose calculation unit are reference values
only. Use them only as a guide.
The calculated values differ from actual dose by up to about 20%1 due to factors
such as distance measurement error, collimator aperture, and X-ray
backscattering. Therefore, the accuracy of displayed values is not guaranteed.
Furthermore, the calculated and actual values can also differ by over 20%1
depending on the imaging region.
*1: Error is with respect to the dosimeter measurement value used in calibration. Due to individual differences in
precision between dosimeters, error values may vary depending on the dosimeter used.
5-10
Wearing a shirt or other clothing may prevent an accurate measurement of

distance.
When measuring distance, do not enter the field of measurement (within a 20 cm

radius from the ranging unit when the field of measurement is at a distance of 1 m
from the focal spot.). Ultrasonic waves are not always radiated in a circular cone
shape. Be sure that persons or objects other than the patient do not enter into the
vicinity of the ultrasonic ranging unit as much as possible. If people or objects
other than the patient enter the field of measurement, distance may be measured
to this secondary person or object rather than to the patient.
When distance cannot be measured, [_ _ _ _ _ _] is displayed.
The dose calculation unit cannot be used concurrently with "5.3 Dose Area
Product Meter" P.5-7.
M503-E027
5.5 Distance Indicator
5.5
Distance Indicator
The distance indicator displays the distance from the focal spot to the surface of the patient. The
distance is measured by the dose calculation unit.
Distance Indicator
5
5
5
5
The display values are reference values only. Use them only as a guide.
Measurement accuracy : 3%
(when measuring distances to concrete or similar hard objects, with no persons or
items in vicinity of ranging unit)
Measurable range: 61 to 266 cm
Wearing a shirt or other clothing may prevent an accurate measurement of

distance.
When measuring distance, do not enter the field of measurement (within a 20 cm

radius from the ranging unit when the field of measurement is at a distance of 1 m
from the focal spot.). Ultrasonic waves are not always radiated in a circular cone
shape. Be sure that persons or objects other than the patient do not enter into the
vicinity of the ultrasonic ranging unit as much as possible. If people or objects
other than the patient enter the field of measurement, distance may be measured
to this secondary person or object rather than to the patient.
When distance cannot be measured, [_ _ _ _ _ _] is displayed.
To use the distance indicator, attach also "5.4 Dose Calculation Unit" P.5-9.
The distance indicator cannot be attached concurrently with "5.3 Dose Area
Product Meter" P.5-7.
When performing oblique or other types of radiography, displayed distance may

be shorter than actual distance.
5
5
5
5
5
M503-E027
5-11
5 Optional Features
5.6
Keyless Entry
The system can be managed using a password instead of a key switch.
The following operations are restricted if a password is not entered.
Electric travel
X-ray exposure
Start up of DR system (only with FPD upgrade)
Protect the password correctly.

Do NOT leave a written copy of the password for others to see, and do NOT
write it on the system.
Turn the power switch on the power supply panel ON
Turning system power ON requires password entry. [P ] will be displayed in the kV

displays on the X-ray control panel until the password is entered.
Use the numeric keypad on the X-ray control panel to enter the correct 4digit password, then press the registration button.
Numeric Keypad
Numeric Delete Button
5-12
After the correct password is entered, electric travel, radiography and the
DR system are enabled.
M503-E027
5.6 Keyless Entry
5
5
The power is automatically switched OFF if an incorrect password is entered three

times.
After the third time an incorrect password is entered, the power is immediately
switched OFF whenever an incorrect password is entered.
If more or less than 4 digits are entered and the registration button is pressed, a
setting error occurs and [P ] [Err] appears in the kV and mAs displays. Try
entering the password again.
Up to 10 passwords can be registered.

User setting parameters can be specified and stored for each password.
If the keyless entry is set, after changing to the user settings mode, [PAS] first
appears on the display. [Pid] does not appears on the display.
If keyless entry is specified, the password must be entered each time the system
is started up.
The password is not checked in the following situations:
The system is restarted within a short time (5 seconds or less) after turning
the power switch OFF
.
The power switch is turned OFF
and ON
to reset an error.
^ Reference "6.2 Malfunction Indicator Lamp" P.6-4
To use the system with a different personal ID, turn the power switch OFF
and wait for at least 5 seconds before turning the power switch ON
again.
Charging the battery is possible only by connecting the power plug. Password
entry is not necessary.
Charging is not possible with the power switch ON
When the auto-power-off function start with a connection of the power plug,
disconnect the power plug to restart the system.
5
5
5
5
5
5
5
M503-E027
5-13
5 Optional Features
5.7
Changing the Grip Bar Height

The grip bar height can be changed to 950 mm, 970 mm, or 1000 mm from the floor surface. Select
the desired height during installation (default bar height is 910 mm).
After changing the grip bar height, be careful not to bump against
anybody or any peripheral articles when moving the system.
Since the grip position is far from the main unit, the ease of rotation changes.
5-14
950 mm
970 mm
1000 mm
M503-E027
5.8 Luminous Hand Switch
5.8
Luminous Hand Switch

The hand switch is illuminated to indicate when the radiography preparation is finished, or that
radiography is in progress.
J Using the Hand Switch
Press the hand switch button to the first level.
5
Illuminated in
Pale Green
5
2
Confirm that the hand switch is illuminated.

When the radiography preparation is finished, the hand switch is illuminated green.
Illuminated Green
5
3
Press the hand switch button to the second level.
X-ray exposure begins.

During exposure, the hand switch is illuminated orange.
Press down on hand switch button continuously until the exposure is finished.
5
Illuminated Orange
5
5
5
5
M503-E027
5-15
5 Optional Features
5.9
Additional Hand Switch

An illuminated hand switch can be added to the front of the system.
During X-ray exposure, use only one of the hand switches.

Though 2 hand switches can be operated at the same time, use only one
hand switch during X-ray radiography in order to avoid unintended exposure.
5-16
M503-E027
5.10 Grid Case
5.10Grid Case
By attaching the grid case, two sheets of grid holder can be stored.
5
5
Grip
5
5
Grid Case
5
5
The grid case is designed to store only the grid holder. If anything other than the
grid holder is stored in the grid case, the case may be broken.
The grip of the grid case option is designed exclusively to open/close the cassette
box. If the grip is used for other purposes, the grip may be broken.
Do not put the cassette in the grid case. Cassette might be exposed.
5
5
5
5
5
5
M503-E027
5-17
5 Optional Features
5.11Large Cassette Box

Large cassette box stores 15 light weight 14 17 inches cassettes.
Large Cassette Box
Step back from the cassette box when opening.

Cassette box might open due to the weight of the cassette.
Cassette box must not be opened during exposure.
Films might be accidentally exposed.
5-18
M503-E027
5.12 FPD Upgrade
5.12FPD Upgrade
5
5
5
5
5
5
5
5
5
If the FPD upgrade is provided, this system cannot expand the grid case or install the largesized cassette box.
For details on the FPD upgrade, see "9 FPD Upgrade" P.9-1.
5
5
5
M503-E027
5-19
Chapter
Troubleshooting
J Chapter Contents
6.1
Warning Indicator Lamp . . . . . . . . . . . . . . . . . . . . . . . .6-2
6.2
Malfunction Indicator Lamp . . . . . . . . . . . . . . . . . . . . . .6-4
6.3
Storing the System for a Long Period . . . . . . . . . . . . . .6-5
6 Troubleshooting
6.1
Warning Indicator Lamp

The
(warning indicator lamp) is illuminated and radiography is disabled under the conditions
described below. The warning code appears on the mAs display for about 3 seconds.
Warning Indicator Lamp
mAs Display
Code
Description
Radiography not possible due to low battery
voltage.
bbb
d0,
Travel system error
d13 to 15
d1 to d3
Motor system error
Solution
Charge the battery.
Immediately stop using the system and contact
your Shimadzu service representative.
If the unit must be moved, do not restore power
to the system. See "4.4 Releasing the Brake in
Emergency" P.4-17.
Immediately stop using the system and contact
your Shimadzu service representative.
Release the brake release bar.
d4
Brake release bar was activated during startup.
d5, d6
Inch-mover button was activated during

startup.
The system can be moved until the lighting of

warning indicator is canceled
although radiography is available.
Release the inch-mover button.
Release the grip bar.
d7, d8
Grip bar was activated during startup.
d9
Obstruction detector was activated during

startup.
d10
An arm lock release button was activated

during startup.

Remove the input to the obstruction detector.
Release the arm lock release button.
6-2

M503-E027
6.1 Warning Indicator Lamp
Code
Description
Solution
Release the arm lock release lever.
d11
Arm lock release lever was activated during

startup.

Stop traveling.
d12
E
EEE
Increased temperature was detected in control

circuit.
Indicates the replacement period for the CPU

memory backup battery.
Warning clears after the control circuit cools

and the temperature falls.
Although normal travel and radiography are
possible, the CPU memory backup battery must
be replaced.
6
6
Contact your Shimadzu service representative.
E5
Indicates the replacement period for the

emergency brake release battery.
Although normal travel and radiography are

possible, the brake cannot be released in an
emergency.
The emergency brake release battery must be
replaced.
Contact your Shimadzu service representative.
F64
F65
Invalid hand switch operation.
F68
X-ray exposure was attempted before DR

radiography preparation was finished.
(Displayed only with FPD upgrade.)
F76
Invalid anatomical code (invalid value) was

sent from DR system. (Displayed only with
FPD upgrade.)
F6d
Emergency stop button was pressed.
Warning clears after the hand switch button is

released.
Wait until DR radiography preparation is

finished before starting radiography.
Warning clears when the FPD radiography
mode button is pressed.
Make the anatomical code correspond with the
anatomical program number.
Under specified radiography parameters

exceeds maximum anode heat content.
Warning clears when a valid value is sent from

the DR system.
Resolve error.
H1
Warning clears when the emergency stop button

is turned in the direction of the arrow and reset.
Reduce radiography parameters, or stop
radiography until the warning indicator lamp
turns OFF.
Warning clears when X-ray tube unit cools
sufficiently.
H2
Maximum anode heat content has reached.
Stop radiography until the warning indicator

lamp turns OFF.
H4
X-ray tube unit temperature is too high.
Warning clears when X-ray tube unit cools

sufficiently.
6
6
6
^ Reference For further details on DR system errors, refer to the Canon CXDI manual (only with FPD
upgrade).
6
M503-E027
6-3
6 Troubleshooting
6.2
Malfunction Indicator Lamp

If the self-diagnostic function detects any malfunction in the system, the
(malfunction indicator
lamp) is illuminated, and radiography is disabled. The malfunction code appears on the mAs display.
If the malfunction indicator lamp is illuminated, switch OFF the power after turning the key switch
to OFF
.
If the malfunction indicator lamp remains illuminated after turning the

power OFF and ON, it indicates that the malfunction still remains. When
this occurs, do NOT operate the system.
If the malfunction indicator lamp turns OFF, but is illuminated
repeatedly, do NOT operate the system. Immediately turn the power
OFF and contact your Shimadzu service representative.
Code
Description
F01, F02
Supply voltage exceeds normal range
F03
Internal power supply circuit error

X-ray tube voltage control error
X-ray exposure is not cancelled if F15 or F16 appear, however, these codes indicate that a tube
voltage control error is detected. If F15 or F16 appears frequently, battery performance may
have deteriorated.
F1*1
X-ray Tube Unit Discharge

The error may be reset by aging the X-ray tube unit.
F14
F2*1
X-ray tube current control error
F3*1
Filament heating control error
F4*1
Capacitor charging control error
F5*1
Battery or charging error

The plug might be connected to the outlet with the main breaker OFF.
Check the status of the main breaker.
F5C
F61
Starter error
F62
Imaging unit error
F6E, F6F
Radiography error
*1: Indicates a number from 0 to 9 or a letter from a to f.

^ Reference For DR system error information, refer to the Canon CXDI manual (only with FPD upgrade).
6-4
M503-E027
6.3 Storing the System for a Long Period
6.3
Storing the System for a Long Period
6
Avoid leaving the system unused for extended periods.
If the system is not to be used for an extended period, follow the procedures below to
reduce battery wear. This does not, however, extend battery life. Shimadzu does not
guarantee the battery life even if the following procedures are implemented.
6
6
J Storage Procedure
1
2
3
Fully charge the battery before storing the system.
After charging, turn the main circuit breaker OFF.

While storing the system, keep the ambient temperature between -10 C
and 40 C.
It is recommended to keep the temperature below 30C.
Recharge battery once every 6 months during storage (given that ambient
temperature is 25 C).
Double this frequency for every 10 C increase in ambient temperature above 25 C.
After storing the system for an extended period, run the system until the
battery indicator displays no illuminated portion, then charge the battery
and repeat this cycle several times to restore battery performance.
6
6
6
6
6
6
M503-E027
6-5
Chapter
Maintenance and
Inspection
J Chapter Contents
7.1
Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-2
7.2
Cleaning the System . . . . . . . . . . . . . . . . . . . . . . . . . . .7-7
7.3
Periodic Replacement Parts . . . . . . . . . . . . . . . . . . . . .7-8
7 Maintenance and Inspection
7.1
7.1.1
Inspection
Daily Inspection
Before using the system, be sure to inspect the following items. If any problems or issues are
discovered, contact your Shimadzu service representative.
Column
X-Ray Tube
Unit
Arm
Arm Joint
Power Supply Panel
Collimator
X-ray Control Panel
Cable
Grip Bar
Hand Switch
No.
7-2
Item
Inspection Point
Appearance
Any cracks, dents, or other damage to the cover?
Grip Bar
Is the grip bar to loose?
M503-E027
7.1 Inspection
No.
Item
Column
Inspection Point
Any abnormal sounds during rotation?
Does the column stop if the arm lock release button or lever is released
during rotation?
Any signs of physical misalignment?
Is the arm joint connected without undue stress?
Any abnormal sounds, looseness, or resistance during up/down, forward/

reverse, or extension/contraction movement?
Does the arm stop if the arm lock release button or lever is released during
up/down, forward/reverse, or extension/contraction movement?
Is the arm to loose when extended to maximum limit?
Is the rail attached below inner arm too loose?
Arm
7
7
7
Arm Joint
7
Inner Arm
Is the top plate loose?
Is the arm catch too loose?
Screws
Arm Joint
Top Plate
Arm Catch
7
6
X-ray Tube Unit
Is X-ray tube unit holder loose?
7
7
7
M503-E027
7-3
No.
Item
Inspection Point
Is the irradiation field made narrow?
Any loose parts in the vicinity of the collimator?
View From A
Screw B
7
Screw A
Collimator
Screws
X-ray Control Panel
Any flickering or abnormal display?
Are the front wheel attachments too loose?
Any physical damage or distortions to the front wheels?
Any abnormal vibrations or sounds when the drive wheels rotate?
Wheels
Screws
10
7-4
Does it appear normal?
Any loose parts?
Does the switch function normally?
M503-E027
7.1 Inspection
No.
Item
11
Inspection Point
Does it appear normal?
Is the grounding cable touching the floor?
Is any debris attached to the cable?
7
7
Grounding Cable
Grounding
Cable
7
Remove dust that has adhered to the belt.
Are any of the plug prongs bent or deformed?
Is the cover damaged or frayed?
Anything abnormal about the power outlet used?
Power Plug
7
12
Power Plug
7
Prongs Not Deformed
13
14
Cables
Wire Rope
No Damage to Cover
Is the cable cover of cable reel damaged or frayed?
Any resistance or unusual noise when reeling the cable in or out?
Any twisting or physical damage of the outer insulation?
Is the wire rope broken?*1
Any strands frayed or damaged?
Any corrosion?
7
7
7
^ Reference "7.1.2 Periodic Inspection" P.7-6
Storage Case
15
16
(only with FPD

upgrade)
Other
Is there any dust on the fan vents?
Do the fan vents exhausted normally?
Any unusual smells or abnormal sounds when the power is turned ON or

while the battery is being charged?
Any abnormal sound or vibration coming from the X-ray tube unit?
Any warning or malfunction indication appears?
7
7
*1: If even a single strand of wire rope is broken, stop using the system and contact your Shimadzu service representative
immediately.
7
M503-E027
7-5
7.1.2 Periodic Inspection

Even if nothing unusual is detected during daily inspections, contact your Shimadzu service
representative to inspect the following items every 6 months:
No.
1
Column
Battery
3
4
Inspection Point
Confirm that all fastener bolts are tight
Any abnormalities in appearance?
Voltage correct?
Power Supply
Is the output voltage normal?
X-ray Output
Confirm X-ray tube voltage, current, and exposure time.
Any frayed or broken strands?
Wire Rope*1
X-ray Tube Rotation
Arm Catch
Arm
10
Grounding Cable
11
Cable
12
7-6
Item
Power Plug
Is the rope secured normally?
Is the rope lubricated?
Any deformation or corrosion?
Are rotating parts lubricated?
Confirm arm stows securely. Is the catch secure?
Is the arm catch too loose?
Confirm storage signal
Any resistance or abnormal sound during up/down movement?
Is appearance normal?
Confirm normal operation
Is appearance normal?
Are any foreign objects attached?
Any twisting or damage to the cable insulation?
Any gap between the plug and stopper?
Are any prongs bent or deformed?
Is the cable cover of cable reel damaged or frayed?
Any resistance or unusual noise when reeling in or out the cable?
Does irradiation field adjusting knob move smoothly?
13
Collimator
*1
Even if wire ropes appear normal during daily inspection, have your Shimadzu service representative replace the
wire rope 10 years after installation. If FPD is upgraded, replace in 7 years.
Shimadzu Part No:
503-64844 (for Type T)
2 cables
503-64844-03 (for Type S)
2 cables
M503-E027
7.2 Cleaning the System
7.2
Cleaning the System

If the system becomes dirty, wipe its outer surfaces with a cloth dampened with a disinfectant.
7
7
When cleaning the system, do NOT allow any liquids inside the cover.
The system is not protected against liquids.
7
7
Never use paint thinners or other organic solvents, other than alcohol for
disinfection.
Film-developing or fixing solutions will cause discoloration.

Wipe off immediately with a damp cloth.
7
7
7
7
7
7
7
7
M503-E027
7-7
7.3
Periodic Replacement Parts

Certain parts should be replaced periodically to ensure the system continues to function properly.
These periodic replacement parts should be installed by your Shimadzu service representative.
If anything unusual is found regarding wire ropes during daily

inspections, contact your Shimadzu service representative.
Battery life varies widely depending on operating conditions. If the
number of uses per charge decreases significantly, it may be due to
the expiration of battery life. Have the battery replaced by your
Shimadzu service representative.
As a general guideline, even if nothing unusual is noticed, replace
the battery every 2 years.
Part Name
7-8
Part No.
Recommended
Replacement Period
Fuse
See next page.
1 year
Halogen Lamp
062-65012-02
1 year
Silicon Packing (for high-voltage generator)
532-23029
1 year
Silicon Packing and Silicon Grease (for X-ray tube unit)
511-15061-13
1 year
Contact Pin
511-15061-11
1 year
Battery (replacement requires 20 units)
074-71014-01
2 years
Wheel
503-48518-01
2 years
Caster, 439S-150
511-37075
2 years
Cable Reel (Power Supply)
503-70591
2 years
Grounding Cable
503-57552
2 years
CPU Backup Battery
074-73307-02
2 years
Battery, Alkaline LR61
074-70020-06
2 years
Relay, G7Z-4A-11Z DC24
065-60052-01
2 years
Relay, G9EA-1-B DC24
065-60053-01
5 years
O-Ring, 4D SS-060
036-11143-21
5 years
SW, Selector HW1K-2B40
064-90066-01
5 years
SW, AVLW32211D-R
064-60785-97
5 years
M503-E027
7.3 Periodic Replacement Parts
Part Name
Recommended
Replacement Period
Part No.
Wheel Cover
503-70351
5 years
Cap for Wheel Cover
541-53637
5 years
Cable Cover
511-18106
5 years
Cable Cover
511-18106-01
5 years
Wire Rope (For Type T)
503-64844
7
7
10 years*1
10 years
*1
Wire Rope (For Type S)
503-64844-03
Motor
511-77098
7500 km
X-Ray Tube Unit
532-24780
30,000 exposures
*1: 7 years if FPD is upgraded.
Fuse Rating List

Unit / Board
DR Unit
(only with FPD upgrade)
Inverter Unit Board*1
Component Name
F21
Current
Rating
Voltage
Rating
2A
250 V
072-01664-26
150 A
600 V
072-06033-10
160 A
660 V
072-06037-11
Part No.
MUX Charge-32K Board
F1
0.5 A
250 V
072-01664-15
MUX Charge-04B Board
F1
5A
250 V
072-01664-33
F1, F2, F10
2A
250 V
072-01664-26
6.25 A
250 V
072-01664-34
F3
MUX Power Board
F4, F5
10 A
250 V
072-01659-83
F6
0.5 A
250 V
072-01664-15
F7, F8
5A
250 V
072-01664-33
F9
10 A
250 V
072-01665-34
F1
6.25 A
250 V
072-01664-34
MUX LC1BF Board
F1
7
7
7
7
*1: For the inverter unit board, select a current rating of either 150 A or 160 A.
7
7
M503-E027
7-9
Chapter
Specifications
J Chapter Contents
8.1
Environmental Conditions of EMC (Electro-Magnetic

Compatibility) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-2
8.2
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-8
8.3
Dimensional Drawings . . . . . . . . . . . . . . . . . . . . . . . .8-16
8.4
X-Ray Tube Unit Reference Axis and Focal Spot Position

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-18
8.5
Radiography Parameters . . . . . . . . . . . . . . . . . . . . . .8-19
8.6
Anatomical Program . . . . . . . . . . . . . . . . . . . . . . . . . .8-23
8.7
Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-37
8.8
Statement of Compliance [For Europe] . . . . . . . . . . . .8-44
8.9
Manufacturer Information . . . . . . . . . . . . . . . . . . . . . .8-46
8 Specifications
8.1
Environmental Conditions of EMC (ElectroMagnetic Compatibility)

The device meets the standard of EMC (Electro-magnetic Compatibility) as shown table.
This device may be affected by electro-magnetic fields. Take care

when using this device in areas where electro-magnetic energy is
present.
Other equipment may be affected due to installation of this device. In
such instances, more the device to avoid problems and interference.
J Classification of EMI in Accordance with EN/IEC 60601-1-2: 2001

Group 1, Class A
The use of ACCESSORIES, transducers and cables other than those

specified, with the exception of transducers and cables sold by the
Shimadzu of the MobileArt Evolution High Power Type (32 kW) as
replacement parts for internal components, may result in increased
EMISSIONS or decreased IMMUNITY of the MobileArt Evolution High
Power Type (32 kW).
J Performance to Be EMC Immunity Tested (Essential Performance)

Essential performances of this equipment are as followings;
8-2
Positioning the X-ray irradiation field
Setting radiography parameters
Irradiating imaging region with X-rays
M503-E027
8.1 Environmental Conditions of EMC (Electro-Magnetic Compatibility)
J Cable List
Table A.1
Cable
Length
Shield
4.0 m
No
Shimadzu Corporation / 503-49045
4.5 m
Yes
Shimadzu Corporation / 511-46381-12
Hand Switch Cable
4.5 m
No
Luminous Hand Switch Cable
4.5 m
No
Additional Protective Grounding Wire
4.2 m
No
Shimadzu Corporation / 501-90150-02
Cable Name
Power Cable
FPD Cable
Note (Manufacturer/Part No.)
8
8
J Option List
Table A.2
Option Type
Note (Manufacturer)
Remote Controller
Shimadzu Corporation
Distance Indicator
Keyless Entry
FPD Upgrade Kit
Wireless LAN
Second FPD kit
8
8
8
8
8
8
8
8
M503-E027
8-3
8 Specifications
J Guidance and Manufacturer's Declaration - Electromagnetic Emissions

Table B.1
Guidance and Manufacturer's Declaration - Electromagnetic Emissions
The MobileArt Evolution High Power Type (32 kW) is intended for use in the electromagnetic environment
specified below. The customer or the user of the MobileArt Evolution High Power Type (32 kW) should
assure that it is used in such an environment.
Emissions Test
RF emissions
EN 55011/
CISPR 11
Group 1
RF emissions
EN 55011/
CISPR 11
Class A
Harmonic emissions
EN 61000-3-2/
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
EN 61000-3-3/
IEC 61000-3-3
8-4
Compliance
Class A
Electromagnetic Environment - Guidance

The MobileArt Evolution High Power Type (32
kW) uses RF energy only for its internal
function. Therefore, its RF emissions are very
low and are not likely to cause any interference
in nearby electronic equipment.
The MobileArt Evolution High Power Type (32

kW) is suitable for use in all establishments other
than domestic and those directly connected to the
public low-voltage power supply network that
supplies buildings used for domestic purposes.
Complies
M503-E027
J Guidance and Manufacturer's Declaration - Electromagnetic Immunity

Table C.1
Guidance and Manufacturer's Declaration - Electromagnetic Immunity

Immunity Test
Electrostatic discharge
(ESD)
EN/IEC 60601
Test Level
Compliance Level
6 kV contact
8 kV air
Electrical fast transient /

burst
2 kV
for power supply lines
2 kV
for power supply lines
EN 61000-4-4/
IEC 61000-4-4
1 kV
1 kV
for input/output lines
for input/output lines
Surge
EN 61000-4-5/
IEC 61000-4-5
Power frequency
(50/60 Hz)
magnetic field
If the floors are covered with

synthetic material, the relative
humidity should be at least
30%.
1 kV line(s) to line(s) 1 kV line(s) to line(s) Mains power quality should be

that of a typical commercial or
2 kV line(s) to earth 2 kV line(s) to earth hospital environment.
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
<5% UT
(>95% dip in UT)
for 5 sec
3 A/m
3 A/m
EN 61000-4-8/
IEC 61000-4-8
Mains power quality should be

hospital environment.
If the user of the MobileArt
Evolution High Power Type (32
kW) requires continued
operation during power mains
interruptions, it is
recommended that the
MobileArt Evolution High
Power Type (32 kW) be
powered from an
uninterruptible power supply or
a battery.
Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical commercial
or hospital environment.
8
8
8
8
8
NOTE
Mains power quality should be

hospital environment.
5% UT
(>95% dip in UT)
for 0.5 cycle
Voltage dips, short
interruptions and voltage
variations on power
supply input lines
EN 61000-4-11/
IEC 61000-4-11
Floors should be wood,

concrete or ceramic tile.
6 kV contact
8 kV air
EN 61000-4-2/
IEC 61000-4-2
Electromagnetic
Environment - Guidance
UT is the a.c. mains voltage prior to application of the test level.
8
8
M503-E027
8-5
8 Specifications
J Guidance and Manufacturer's Declaration - Electromagnetic Immunity

Table C.2
Guidance and Manufacturer's Declaration - Electromagnetic Immunity
Immunity Test
EN/
IEC 60601
Test Level
Compliance
Level
Electromagnetic Environment - Guidance
Portable and mobile RF communications equipment

should be used no closer to any part of the MobileArt
Evolution High Power Type (32 kW), including cables,
than the recommended separation distance calculated from
the equation applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6/
IEC 61000-4-6
3 Vrms
150 kHz to
80 MHz
3 Vrms
d = 1.2 P
Radiated RF
EN 61000-4-3/
IEC 61000-4-3
3 V/m
80 MHz to
2.5 GHz
3 V/m
d = 1.2 P 80 MHz to 800 MHz

d = 2.3 P 800 MHz to 2.5 GHz
where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmitters, as determined
by an electromagnetic site survey*1, should be less than
the compliance level in each frequency range*2.
Interference may occur in the vicinity of equipment
marked with the following symbol:
NOTE
At 80 MHz and 800 MHz, the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
*1: Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the MobileArt Evolution High Power Type (32 kW)
is used exceeds the applicable RF compliance level above, the MobileArt Evolution High Power Type (32 kW) should
be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as reorienting or relocating the MobileArt Evolution High Power Type (32 kW).
*2: Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
8-6
M503-E027
J Recommended Separation Distances between Portable and Mobile

RF Communications Equipment and the EQUIPMENT or SYSTEM
Table D.2
Recommended Separation Distances between Portable
and Mobile RF Communications Equipment and the MobileArt Evolution High Power Type (32 kW)
The MobileArt Evolution High Power Type (32 kW) is intended for use in an electromagnetic environment in
which radiated RF disturbances are controlled.
The customer or the user of the MobileArt Evolution High Power Type (32 kW) can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the MobileArt Evolution High Power Type (32 kW) as
recommended below, according to the maximum output power of the communications equipment.
Separation Distance According to Frequency of Transmitter (m)
Rated Maximum
Output Power of
Transmitter
(W)
150 kHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2.5 GHz
d = 1.2 P
d = 1.2 P
d = 2.3 P
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
8
8
8
NOTE
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in
meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
8
8
8
8
8
8
8
M503-E027
8-7
8 Specifications
8.2
Specifications
Two types of MobileArt Evolution High Power Type (32 kW) are available, each with different
column heights.
Type
8.2.1
Column Height
Type S
1780 mm
Type T
1930 mm
Operating Environment
Item
Ambient Temperature

Relative Humidity
8.2.2
Specification
700 hPa to 1060 hPa
Power Supply
Item
When Powered
by Battery
Specification
Power Supply
Internal battery
Battery Type
Sealed lead storage battery (12 V 20 cells)
Power Supply Rating 1 kVA
When Charging
Battery
Supply Voltage
Single phase 100, 110, 120, 200, 220, 230, 240 V AC
Supply Frequency
50/60 Hz
Single phase 100, 110, 120 V AC: 1.0 max.
Supply Impedance
Single phase 200, 220, 230, 240 V AC: 4.0 max.

Ground terminal: 100 max.
Ground Resistance
Power Cable Length
8-8
Additional ground terminal: 100 max.

4m
M503-E027
8.2 Specifications
8.2.3
High-Voltage Generator
Item
8
Specification
JIS Compliant Model
BIR-320-133
Max. Electric Power
32 kW (100 kV, 320 mA, 20 ms / 80 kV, 400 mA, 20 ms)

16 kW (100 kV, 160 mA, 0.1 s)
Nominal Electric Power
(product of max current flow possible for 0.1 seconds and tube
voltage, at 100 kV nominal tube voltage)
Ratings
Nominal maximum tube voltage and

maximum tube current where nominal
maximum tube voltage output is possible:
133 kV, 200 mA
Maximum tube current and maximum tube

voltage where maximum tube current
output is possible:
400 mA, 80 kV
Combination of tube voltage and tube

current that outputs maximum electrical
power:
100 kV, 320 mA /

80 kV, 400 mA
Minimum current-time product:
0.32 mAs
Maximum current-time product:
320 mAs
8
8
8
Nominal minimum irradiation time: 1 msec
Settings Possible at
Given Cassette
Radiography Voltage
Given (Low Battery
mode) Cassette
Radiography Voltage
Given DR Long-Term
Exposure Mode Voltage
(only with FPD
upgrade)
Large
Focus
Small
Focus
Common
with
Large
Focus
and
Small
Focus
Large
Focus
40 to 90 kV:
0.32 to 320 mAs
101 to 110 kV: 0.32 to 250 mAs
91 to 100 kV:
0.32 to 280 mAs
111 to 120 kV: 0.32 to 220 mAs
40 to 90 kV:
0.32 to 320 mAs
101 to 110 kV: 0.32 to 250 mAs
91 to 100 kV:
0.32 to 280 mAs
111 to 120 kV: 0.32 to 220 mAs
91 to 100 kV:
111 to 120 kV: 0.32 to 220 mAs
8
8
121 to 133 kV: 0.32 to 200 mAs
40 to 90 kV:
0.32 to 320 mAs
101 to 110 kV: 0.32 to 250 mAs
0.32 to 280 mAs
121 to 133 kV: 0.32 to 200 mAs
40 to 65 kV:
0.32 to 320 mAs
66 to 80 kV:
0.32 to 280 mAs
81 to 85 kV:
0.32 to 250 mAs
86 to 100 kV:
0.32 to 220 mAs
101 to 105 kV: 0.32 to 200 mAs
106 to 125 kV: 0.32 to 180 mAs
126 to 133 kV: 0.32 to 140 mAs

Small
Focus
121 to 133 kV: 0.32 to 200 mAs
40 to 65 kV:
0.32 to 320 mAs
66 to 80 kV:
0.32 to 280 mAs
81 to 100 kV:
0.32 to 220 mAs
101 to 125 kV: 0.32 to 180 mAs
126 to 133 kV: 0.32 to 140 mAs
8
8
M503-E027
8-9
8 Specifications
Item
Given DR Radiography
Voltage
(only with FPD
upgrade)
Given (Low Battery
mode) DR Long-Term
Exposure Mode Voltage
(only with FPD
upgrade)
Specification
Large
Focus
40 to 50 kV:
0.32 to 200 mAs
51 to 60 kV:
0.32 to 160 mAs
61 to 80 kV:
0.32 to 125 mAs
81 to 100 kV:
0.32 to 100 mAs
101 to 125 kV: 0.32 to 80 mAs

131 to 133 kV: 0.32 to 50 mAs
Small
Focus
40 to 60 kV:
0.32 to 160 mAs
61 to 80 kV:
81 to 100 kV:
0.32 to 100 mAs
101 to 125 kV: 0.32 to 80 mAs
126 to 130 kV: 0.32 to 63 mAs
Common
with
40 to 65 kV:
0.32 to 320 mAs
Large
81 to 100 kV: 0.32 to 220 mAs
Focus
and
121 to 133 kV: 0.32 to 140 mAs
Small
Focus
(only with FPD

upgrade)
Large
Focus
0.32 to 125 mAs
131 to 133 kV: 0.32 to 50 mAs
66 to 80 kV:
0.32 to 280 mAs
101 to 120 kV: 0.32 to 180 mAs
0.32 to 200 mAs
51 to 55 kV:
0.32 to 160 mAs
56 to 65 kV:
0.32 to 125 mAs
66 to 80 kV:
0.32 to 100 mAs
81 to 100 kV:
0.32 to 80 mAs
101 to 120 kV: 0.32 to 63 mAs
40 to 50 kV:
Given (Low Battery
mode) DR Radiography
Voltage
126 to 130 kV: 0.32 to 63 mAs
121 to 133 kV: 0.32 to 50 mAs

Small
Focus
Tube Voltage Setting Range and

Display
Current-Time Product Setting Range

and Display
40 to 55 kV:
0.32 to 160 mAs
56 to 65 kV:
0.32 to 125 mAs
66 to 80 kV:
0.32 to 100 mAs
81 to 100 kV:
0.32 to 80 mAs
101 to 120 kV: 0.32 to 63 mAs
121 to 133 kV: 0.32 to 50 mAs
Setting Range: 40 kV to 133 kV, in 1 kV increments

Display:
Digital
Setting Range: 0.32, 0.36, 0.40, 0.45, 0.50, 0.56, 0.63, 0.71, 0.80,
0.90, 1.0, 1.1, 1.2, 1.4, 1.6, 1.8, 2.0, 2.2, 2.5, 2.8, 3.2,
3.6, 4.0, 4.5, 5.0, 5.6, 6.3, 7.1, 8.0, 9.0, 10, 11, 12, 14,
16, 18, 20, 22, 25, 28, 32, 36, 40, 45, 50, 56, 63, 71,
80, 90, 100, 110, 125, 140, 160, 180, 200, 220, 250,
280, 320 mAs
Display:
Digital
A total of 144 types of anatomical programs can be registered, using 8

imaging portions, 3 directions, 3 body thicknesses, and 2 radiography
mode (8 3 3 2 = 144).
The following radiography parameters can be registered in anatomical
programs.
Anatomical Programs
Only after FPD upgrade kit (1panel) installed up to 144 anatomical

programs.
(8 regions 3 orientations 3 body thicknesses 2 = 144)
Only after FPD upgrade kit (2panel) or Second FPD kit installed up to
216 anatomical programs.
(8 regions 3 orientations 3 body thicknesses 3 = 216)
8-10
M503-E027
8.2 Specifications
8.2.4
X-ray Tube Unit
Item
Specification
Model
0.7/1.3U163C-36
Nominal Focal Spot Size
0.7/1.3 mm
Target Angle
16 degrees
Nominal Max.
Tube Voltage
X-ray Tube
Unit (tube and
housing)
X-ray Tube
(tube only)
Weight
Radiography
133 kV
Max. Heat Content
750 kJ (1060 kHU)
Max. Continuous
Heat Dissipation
Rate
120 W (170 HU/s)
Max. Anode Heat

Content
210 kJ (300 kHU)
Max. Anode Heat

Dissipation Rate
800 W (1130 HU/s)
Max. Continuous
Heat Dissipation
Rate
210 W (300 HU/s)
8
8
8
8
8
12.8 kg
8
8
8
8
8
8
8
M503-E027
8-11
8 Specifications
8.2.5
Collimator
Item
Model
Specification
R-20C
Field
Shape
Rectangular
Max. Field
430 mm 430 mm at SID 1 m
Min. Field
0 mm 0 mm (leaves closed)
Average Illumination 160 lx min.

Illuminance Ratio
3 min.
Precision
2% of SID
Center Indicator
Cross hairs
Type Of Lamp
Halogen lamp (JM12 V 100 W 10 H)
Illumination Period
30 seconds max., with automatic off timer
SID Display
1, 1.5, 2 m
Dimensions Display
20 (8), 23 (9), 25 (10), 28 (11), 30 (12), 36 (14), 43 (17) cm (in.)
Illuminated Field
Field Size
Indicator
8.2.6
Leaf Movement
Manual
Focal Length (distance between focal

spot and collimator attachment surface,
when installed)
56 mm
External Dimensions
202 mm 211 mm 200 mm
X-ray Tube Unit Holder

Item
Focal Spot Height
8-12
Specification
Type S: 600 mm to 1860 mm
Type T: 600 mm to 2010 mm
Arm Length
635 mm to 1200 mm
Column Rotation Range
270 degrees
X-ray Tube Rotation Angle
180 degrees
X-ray Tube Axial Rotation
Forward 90 degrees, backward 20 degrees
M503-E027
8.2 Specifications
8.2.7
Minimum Inherent Filtration

Item
8
Specification
Total
2.5 mm Al at 70 kV
X-ray Tube Unit
1.5 mm Al equivalent at 70 kV
Collimator
1.0 mm Al equivalent at 70 kV
8
8.2.8
DR System (Only with FPD Upgrade)
8
Item
Application
Specification
General X-ray radiography
CXDI-50G/50C
FPD
CXDI-55G/55C
CXDI-60G/60C
Scintillator
Pixel Size
Effective Number Of Pixels
CXDI-50G/55G/60G : GOS
CXDI-50C/55C/60C : CsI
160 m 160 m
CXDI-50G/50C/55G/55C: 2208 2688 (about 5.9 megapixels)
CXDI-60G/60C
: 1464 1776 (about 2.6 megapixels)
Automatic irradiation field recognition

Effective Irradiation Range
CXDI-50G/50C/55G/55C: 35 cm 43 cm max.
CXDI-60G/60C
DR
Dynamic Range
About 4-digit level
Gradation
12 bit (4096 gradations)
Max. Exposure Time
3000 msec
: 23 cm 28 cm max.
CXDI-50G/50C : 4.8 kg
Weight
CXDI-55G/55C : 3.4 kg (without cable)
CXDI-60G/60C : 2.5 kg (without cable)

Mechanical Strength
Partial load: 100 kg, given 40 mm diameter

Uniform load: 150 kg over all surfaces
CXDI-50G/50C : W491 mm D477 mm H23 mm

External Dimensions
CXDI-55G/55C : W480 mm D481 mm H15 mm

CXDI-60G/60C : W344 mm D380 mm H22.5 mm
Display
Unit
Size
15 inches
8
M503-E027
8-13
8 Specifications
8.2.9
Options
Item
Specification
Infrared type
Remote Controller
Grid Unit
Attaches to front of imaging unit.
Protective Screen (folding)
Folding protective acrylic X-ray screen
Indicates the dose-area product (cannot be installed together with

the dose calculation unit or the distance indicator).
Calculates and displays the radiation dosage of the X-ray applied

to surface of the patient (cannot be installed together with dose
area product meter).
Distance Indicator
Shows the distance measured by the dose calculation unit

(cannot be installed together with dose area product meter).
Keyless Entry
The system can be managed using a password instead of a key

switch.
Changing the Grip Bar Height
The grip bar height can be changed to 950 mm, 970 mm, or
1000 mm from floor surface.
The hand switch illuminates to indicate when radiography

preparation is finished, or that radiography is in progress.
Allows adding an illuminated hand switch to front of system.
Wireless LAN
By installing a commercial wireless LAN adapter (USB

connection-type), wireless LAN function can be used.
Grid Case
By attaching the grid case, two sheets of grid holder can be stored.
Large Cassette Box
The large cassette box stores 15 light weight 14 17 inches

cassettes.
FPD Upgrade
Allows adding DR system to this system.
Second FPD kit
2 imaging units are available by this kit. Imaging units are

alternated by detachable connector.

FPD bag
8-14
Radiography preparation, X-ray exposure, collimator lamp ON/

OFF
This bag allows the imaging unit to slide smoothly.
M503-E027
8.2 Specifications
8.2.10 Custom Specifications
Item
Focal Spot Lift
(only for Type S)
Specification
Lifts focal spot up by 150 mm (focal spot height 750 mm to

2010 mm).
Note: Custom specifications cannot be changed after delivery.
8
8
8
8
8
8
8
8
8
8
8
M503-E027
8-15
8 Specifications
8.3
8.3.1
Dimensional Drawings
General Dimensions
Item
Specification
Total Width
580 mm
Total Length
1220 mm (only with FPD upgrade: 1220 mm)
Height of Column
Type S: 1780 mm
Type T: 1930 mm
Weight
390 kg (only with FPD upgrade: 420 kg)
Maximum Travel Speed
Approx. 5 km/h (may vary depending on condition)
Values shown in (
8-16
) are for Type S
M503-E027
8.3 Dimensional Drawings
With FPD Upgrade
8
8
8
8
8
Values shown in (
) are for Type S.
8
8
8
8
8
8
8
8
M503-E027
8-17
8 Specifications
8.4
X-Ray Tube Unit Reference Axis and Focal

Spot Position
X-ray Tube Unit Focal Spot Position (Top View)
Focal Spot1
Reference Axis
372
1: Focal spot is indicated by a mark on the X-ray tube unit surface.
Unit: mm
X-ray Tube Unit Focal Spot Position (Side View)
Focal Spot
Reference Axis
8-18
Unit: mm
M503-E027
8.5 Radiography Parameters
8.5
8.5.1
Radiography Parameters
Normal Use
J Large Focus
Tube
CurrentTime
Product
(mAs)
Tube Voltage (kV)
133
125
100
80
60
40
0.32
0.0016
0.0012
0.0010
0.0010
0.0010
0.0012
0.5
0.0025
0.0020
0.0016
0.0012
0.0016
0.0020
0.0050
0.0040
0.0032
0.0025
0.0032
0.0040
0.0100
0.0080
0.0063
0.0050
0.0063
0.0080
0.040
0.020
0.016
0.012
0.016
0.020
0.080
0.063
0.040
0.020
0.025
0.032
10
0.100
0.080
0.063
0.040
0.032
0.040
16
0.320
0.200
0.100
0.080
0.063
0.063
20
0.400
0.250
0.200
0.100
0.080
0.080
50
1.00
0.63
0.50
0.40
0.32
0.25
100
2.00
1.25
1.00
0.80
0.63
0.50
200
4.00
3.20
2.50
2.00
1.25
1.00
320
3.20
2.50
1.60
(Unit: sec)
8
8
8
8
8
8
8
8
8
M503-E027
8-19
8 Specifications
J Small Focus
Tube
CurrentTime
Product
(mAs)
Tube Voltage (kV)
133
125
100
80
60
40
0.32
0.0032
0.0025
0.0020
0.0016
0.0016
0.0020
0.5
0.0050
0.0040
0.0032
0.0025
0.0025
0.0032
0.0100
0.0080
0.0063
0.0050
0.0050
0.0063
0.0200
0.0160
0.0120
0.0100
0.0100
0.0120
0.006
0.006
0.040
0.032
0.025
0.032
0.100
0.100
0.063
0.050
0.050
0.050
10
0.125
0.125
0.080
0.063
0.063
0.063
16
0.320
0.200
0.125
0.100
0.100
0.100
20
0.400
0.250
0.200
0.125
0.125
0.125
50
1.00
0.63
0.50
0.40
0.32
0.32
100
2.00
1.60
1.00
0.80
0.63
0.63
200
4.00
3.20
2.50
2.00
1.25
1.25
320
3.20
2.50
2.00
(Unit: sec)
8-20
M503-E027
8.5 Radiography Parameters
8.5.2
Low-Battery Mode
J Large Focus
Tube
CurrentTime
Product
(mAs)
Tube Voltage (kV)
133
125
100
80
60
40
0.32
0.0016
0.0012
0.0010
0.0010
0.0010
0.0012
0.5
0.0025
0.0020
0.0016
0.0012
0.0016
0.0020
0.0050
0.0040
0.0032
0.0025
0.0032
0.0040
0.0100
0.0080
0.0063
0.0050
0.0063
0.0080
0.040
0.020
0.016
0.012
0.016
0.020
0.160
0.080
0.040
0.020
0.025
0.032
10
0.200
0.160
0.080
0.040
0.032
0.040
16
0.320
0.320
0.200
0.160
0.100
0.063
20
0.400
0.400
0.250
0.200
0.160
0.080
50
1.00
1.00
0.63
0.50
0.40
0.25
100
2.00
2.00
1.25
1.00
0.80
0.50
200
4.00
4.00
2.50
2.00
1.60
1.00
320
3.20
2.50
1.60
(Unit: sec)
8
8
8
8
8
8
8
8
8
8
M503-E027
8-21
8 Specifications
J Small Focus
Tube
CurrentTime
Product
(mAs)
Tube Voltage (kV)
133
125
100
80
60
40
0.32
0.0032
0.0025
0.0020
0.0016
0.0016
0.0020
0.5
0.0050
0.0040
0.0032
0.0025
0.0025
0.0032
0.0100
0.0080
0.0063
0.0050
0.0050
0.0063
0.0200
0.0160
0.0120
0.0100
0.0100
0.0120
0.100
0.100
0.063
0.040
0.025
0.032
0.160
0.160
0.100
0.080
0.063
0.050
10
0.200
0.200
0.125
0.100
0.080
0.063
16
0.320
0.320
0.200
0.160
0.125
0.100
20
0.400
0.400
0.250
0.200
0.160
0.125
50
1.00
1.00
0.63
0.50
0.40
0.32
100
2.00
2.00
1.25
1.00
0.80
0.63
200
4.00
4.00
2.50
2.00
1.60
1.25
320
3.20
2.50
2.00
(Unit: sec)
8-22
M503-E027
8.6 Anatomical Program
8.6
8.6.1
Anatomical Program
Anatomical Program
The factory-set anatomical program numbers (APR numbers) and their radiography parameters are
indicated below.
APR for Chest and leg are set 32 kw electric power, using the large focus, to minimize image blur
from body movement. Exposure time may be extended and tube current decreases in some
radiography settings when choosing the small focus.
Electric power* of High mAs settings like APR for Abdomen and Waist have no difference between
the large and small focus.
8
8
* Electric power mean kV times mAs.
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
Head
Frontal
Thin
64
14
Small
Head
Frontal
Normal
64
14
Small
Head
Frontal
Thick
66
16
Small
Head
Lateral
Thin
56
14
Small
Head
Lateral
Normal
58
14
Small
Head
Lateral
Thick
61
14
Small
Head
Oblique
Thin
56
18
Small
Head
Oblique
Normal
59
18
Small
Head
Oblique
Thick
62
18
Small
10
Chest
Frontal
Thin
79
2.8
Large
11
Chest
Frontal
Normal
79
3.2
Large
12
Chest
Frontal
Thick
82
3.2
Large
13
Chest
Lateral
Thin
88
3.2
Large
14
Chest
Lateral
Normal
91
3.6
Large
15
Chest
Lateral
Thick
95
Large
16
Chest
Oblique
Thin
87
3.2
Large
17
Chest
Oblique
Normal
90
3.2
Large
18
Chest
Oblique
Thick
93
3.2
Large
19
Abdomen
Frontal
Thin
74
56
Small
20
Abdomen
Frontal
Normal
77
63
Small
21
Abdomen
Frontal
Thick
80
71
Small
8-23
8
8
8
8
8
8
8
8
8
8 Specifications
8-24
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
22
Abdomen
Lateral
Thin
86
63
Small
23
Abdomen
Lateral
Normal
90
63
Small
24
Abdomen
Lateral
Thick
95
63
Small
25
Abdomen
Oblique
Thin
78
80
Small
26
Abdomen
Oblique
Normal
83
80
Small
27
Abdomen
Oblique
Thick
89
80
Small
28
Waist
Frontal
Thin
68
22
Small
29
Waist
Frontal
Normal
68
25
Small
30
Waist
Frontal
Thick
71
25
Small
31
Waist
Lateral
Thin
82
22
Small
32
Waist
Lateral
Normal
84
25
Small
33
Waist
Lateral
Thick
86
28
Small
34
Waist
Oblique
Thin
71
22
Small
35
Waist
Oblique
Normal
74
25
Small
36
Waist
Oblique
Thick
76
28
Small
37
Leg
Frontal
Thin
63
7.1
Large
38
Leg
Frontal
Normal
63
Large
39
Leg
Frontal
Thick
66
Large
40
Leg
Lateral
Thin
65
7.1
Large
41
Leg
Lateral
Normal
68
7.1
Large
42
Leg
Lateral
Thick
71
7.1
Large
43
Leg
Oblique
Thin
65
Large
44
Leg
Oblique
Normal
65
Large
45
Leg
Oblique
Thick
65
10
Large
46
Foot
Frontal
Thin
58
2.2
Small
47
Foot
Frontal
Normal
58
2.5
Small
48
Foot
Frontal
Thick
61
2.5
Small
49
Foot
Lateral
Thin
57
Small
50
Foot
Lateral
Normal
58
Small
51
Foot
Lateral
Thick
61
Small
52
Foot
Oblique
Thin
55
2.5
Small
53
Foot
Oblique
Normal
58
2.5
Small
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
54
Foot
Oblique
Thick
61
2.8
Small
55
Arm
Frontal
Thin
58
2.8
Small
56
Arm
Frontal
Normal
58
3.2
Small
57
Arm
Frontal
Thick
61
3.2
Small
58
Arm
Lateral
Thin
61
2.8
Small
59
Arm
Lateral
Normal
63
3.2
Small
60
Arm
Lateral
Thick
65
3.6
Small
61
Arm
Oblique
Thin
60
3.2
Small
62
Arm
Oblique
Normal
60
3.6
Small
63
Arm
Oblique
Thick
60
Small
64
Hand
Frontal
Thin
53
0.9
Small
65
Hand
Frontal
Normal
53
Small
66
Hand
Frontal
Thick
56
Small
67
Hand
Lateral
Thin
56
0.9
Small
68
Hand
Lateral
Normal
58
0.9
Small
69
Hand
Lateral
Thick
60
0.9
Small
70
Hand
Oblique
Thin
56
Small
71
Hand
Oblique
Normal
57
Small
72
Hand
Oblique
Thick
57
1.1
Small
8
8
8
8
8
8
8
8
8
8
8
8
8
M503-E027
8-25
8 Specifications
8.6.2
Anatomical Program Number (Only with FPD upgrade)

The factory-set anatomical program numbers (APR numbers) and their radiography parameters are
indicated below.
APR for Chest and leg are set 32 kw electric power, using the large focus, to minimize image blur
from body movement. Exposure time may be extended and tube current decreases in some
radiography settings when choosing the small focus.
Electric power* of High mAs settings like APR for Abdomen and Waist have no difference between
the large and small focus.
APR Numbers 1 to 72 are number of CXDI-50G/50C/55G/55C's APR Number. APR Numbers 73 to
144 are number of CXDI-60G/60C's APR Number.
If APR Number 1 to 72 selected,
illuminated.
FPD/Cassette Radiography Mode Button's Right LED is
If APR Number 73 to 144 selected,

blinked.
FPD/Cassette Radiography Mode Button's Right LED is
* Electric power mean kV times mAs.

CXDI-50G/55G
8-26
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
Head
Frontal
Thin
64
14
Small
Head
Frontal
Normal
64
14
Small
Head
Frontal
Thick
66
16
Small
Head
Lateral
Thin
56
14
Small
Head
Lateral
Normal
58
14
Small
Head
Lateral
Thick
61
14
Small
Head
Oblique
Thin
56
18
Small
Head
Oblique
Normal
59
18
Small
Head
Oblique
Thick
62
18
Small
10
Chest
Frontal
Thin
79
2.8
Large
11
Chest
Frontal
Normal
79
3.2
Large
12
Chest
Frontal
Thick
82
3.2
Large
13
Chest
Lateral
Thin
88
3.2
Large
14
Chest
Lateral
Normal
91
3.6
Large
15
Chest
Lateral
Thick
95
Large
16
Chest
Oblique
Thin
87
3.2
Large
17
Chest
Oblique
Normal
90
3.2
Large
18
Chest
Oblique
Thick
93
3.2
Large
19
Abdomen
Frontal
Thin
74
56
Small
M503-E027
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
20
Abdomen
Frontal
Normal
77
63
Small
21
Abdomen
Frontal
Thick
80
71
Small
22
Abdomen
Lateral
Thin
86
63
Small
23
Abdomen
Lateral
Normal
90
63
Small
24
Abdomen
Lateral
Thick
95
63
Small
25
Abdomen
Oblique
Thin
78
80
Small
26
Abdomen
Oblique
Normal
83
80
Small
27
Abdomen
Oblique
Thick
89
80
Small
28
Waist
Frontal
Thin
68
22
Small
29
Waist
Frontal
Normal
68
25
Small
30
Waist
Frontal
Thick
71
25
Small
31
Waist
Lateral
Thin
82
22
Small
32
Waist
Lateral
Normal
84
25
Small
33
Waist
Lateral
Thick
86
28
Small
34
Waist
Oblique
Thin
71
22
Small
35
Waist
Oblique
Normal
74
25
Small
36
Waist
Oblique
Thick
76
28
Small
37
Leg
Frontal
Thin
63
7.1
Large
38
Leg
Frontal
Normal
63
Large
39
Leg
Frontal
Thick
66
Large
40
Leg
Lateral
Thin
65
7.1
Large
41
Leg
Lateral
Normal
68
7.1
Large
42
Leg
Lateral
Thick
71
7.1
Large
43
Leg
Oblique
Thin
65
Large
44
Leg
Oblique
Normal
65
Large
45
Leg
Oblique
Thick
65
10
Large
46
Foot
Frontal
Thin
58
2.2
Small
47
Foot
Frontal
Normal
58
2.5
Small
48
Foot
Frontal
Thick
61
2.5
Small
49
Foot
Lateral
Thin
57
Small
50
Foot
Lateral
Normal
58
Small
51
Foot
Lateral
Thick
61
Small
8-27
8
8
8
8
8
8
8
8
8
8
8
8
8
8 Specifications
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
52
Foot
Oblique
Thin
55
2.5
Small
53
Foot
Oblique
Normal
58
2.5
Small
54
Foot
Oblique
Thick
61
2.8
Small
55
Arm
Frontal
Thin
58
2.8
Small
56
Arm
Frontal
Normal
58
3.2
Small
57
Arm
Frontal
Thick
61
3.2
Small
58
Arm
Lateral
Thin
61
2.8
Small
59
Arm
Lateral
Normal
63
3.2
Small
60
Arm
Lateral
Thick
65
3.6
Small
61
Arm
Oblique
Thin
60
3.2
Small
62
Arm
Oblique
Normal
60
3.6
Small
63
Arm
Oblique
Thick
60
Small
64
Hand
Frontal
Thin
53
0.9
Small
65
Hand
Frontal
Normal
53
Small
66
Hand
Frontal
Thick
56
Small
67
Hand
Lateral
Thin
56
0.9
Small
68
Hand
Lateral
Normal
58
0.9
Small
69
Hand
Lateral
Thick
60
0.9
Small
70
Hand
Oblique
Thin
56
Small
71
Hand
Oblique
Normal
57
Small
72
Hand
Oblique
Thick
57
1.1
Small
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
Head
Frontal
Thin
64
7.1
Small
Head
Frontal
Normal
64
Small
Head
Frontal
Thick
66
Small
Head
Lateral
Thin
56
7.1
Small
Head
Lateral
Normal
58
7.1
Small
Head
Lateral
Thick
61
7.1
Small
Head
Oblique
Thin
56
Small
CXDI-50C/55C
8-28
M503-E027
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
Head
Oblique
Normal
59
Small
Head
Oblique
Thick
62
Small
10
Chest
Frontal
Thin
79
1.4
Large
11
Chest
Frontal
Normal
79
1.6
Large
12
Chest
Frontal
Thick
82
1.6
Large
13
Chest
Lateral
Thin
88
1.6
Large
14
Chest
Lateral
Normal
91
1.8
Large
15
Chest
Lateral
Thick
95
Large
16
Chest
Oblique
Thin
87
1.6
Large
17
Chest
Oblique
Normal
90
1.6
Large
18
Chest
Oblique
Thick
93
1.6
Large
19
Abdomen
Frontal
Thin
74
28
Small
20
Abdomen
Frontal
Normal
77
32
Small
21
Abdomen
Frontal
Thick
80
36
Small
22
Abdomen
Lateral
Thin
86
32
Small
23
Abdomen
Lateral
Normal
90
32
Small
24
Abdomen
Lateral
Thick
95
32
Small
25
Abdomen
Oblique
Thin
78
40
Small
26
Abdomen
Oblique
Normal
83
40
Small
27
Abdomen
Oblique
Thick
89
40
Small
28
Waist
Frontal
Thin
68
11
Small
29
Waist
Frontal
Normal
68
12
Small
30
Waist
Frontal
Thick
71
12
Small
31
Waist
Lateral
Thin
82
11
Small
32
Waist
Lateral
Normal
84
12
Small
33
Waist
Lateral
Thick
86
14
Small
34
Waist
Oblique
Thin
71
11
Small
35
Waist
Oblique
Normal
74
12
Small
36
Waist
Oblique
Thick
76
14
Small
37
Leg
Frontal
Thin
63
3.6
Large
38
Leg
Frontal
Normal
63
Large
39
Leg
Frontal
Thick
66
Large
8-29
8
8
8
8
8
8
8
8
8
8
8
8
8
8 Specifications
8-30
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
40
Leg
Lateral
Thin
65
3.6
Large
41
Leg
Lateral
Normal
68
3.6
Large
42
Leg
Lateral
Thick
71
3.6
Large
43
Leg
Oblique
Thin
65
Large
44
Leg
Oblique
Normal
65
4.5
Large
45
Leg
Oblique
Thick
65
Large
46
Foot
Frontal
Thin
58
1.1
Small
47
Foot
Frontal
Normal
58
1.2
Small
48
Foot
Frontal
Thick
61
1.2
Small
49
Foot
Lateral
Thin
57
Small
50
Foot
Lateral
Normal
58
Small
51
Foot
Lateral
Thick
61
Small
52
Foot
Oblique
Thin
55
1.2
Small
53
Foot
Oblique
Normal
58
1.2
Small
54
Foot
Oblique
Thick
61
1.4
Small
55
Arm
Frontal
Thin
58
1.4
Small
56
Arm
Frontal
Normal
58
1.6
Small
57
Arm
Frontal
Thick
61
1.6
Small
58
Arm
Lateral
Thin
61
1.4
Small
59
Arm
Lateral
Normal
63
1.6
Small
60
Arm
Lateral
Thick
65
1.8
Small
61
Arm
Oblique
Thin
60
1.6
Small
62
Arm
Oblique
Normal
60
1.8
Small
63
Arm
Oblique
Thick
60
Small
64
Hand
Frontal
Thin
53
0.45
Small
65
Hand
Frontal
Normal
53
0.5
Small
66
Hand
Frontal
Thick
56
0.5
Small
67
Hand
Lateral
Thin
56
0.45
Small
68
Hand
Lateral
Normal
58
0.45
Small
69
Hand
Lateral
Thick
60
0.45
Small
70
Hand
Oblique
Thin
56
0.5
Small
71
Hand
Oblique
Normal
57
0.5
Small
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
72
Hand
Oblique
Thick
57
0.56
Small
CXDI-60G
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
73
Head
Frontal
Thin
64
14
Small
74
Head
Frontal
Normal
64
16
Small
75
Head
Frontal
Thick
66
16
Small
76
Head
Lateral
Thin
56
14
Small
77
Head
Lateral
Normal
58
14
Small
78
Head
Lateral
Thick
61
14
Small
79
Head
Oblique
Thin
56
18
Small
80
Head
Oblique
Normal
59
18
Small
81
Head
Oblique
Thick
62
18
Small
82*1
Chest
52
2.2
Large
83*1
Chest
55
2.5
Large
84*1
Chest
57
2.8
Large
59
2.8
Large
60
2.8
Large
*1
M503-E027
Infant
(Frontal/Thin)
1 and 2-year-old
(Frontal/Normal)
3 to 6-year-old
(Frontal/Thick)
7 to 9-year-old
85
Chest
86*1
Chest
87
Chest
Lateral
Thick
95
Large
88
Chest
Oblique
Thin
87
3.2
Large
89
Chest
Oblique
Normal
90
3.2
Large
90
Chest
Oblique
Thick
93
3.2
Large
91*1
Abdomen
50
2.2
Small
92*1
Abdomen
52
2.5
Small
93*1
Abdomen
55
2.8
Small
94*1
Abdomen
58
3.2
Small
(Lateral/Thin)
10 to 12-year-old
(Lateral/Normal)
Infant
(Frontal/Thin)
1 and 2-year-old
(Frontal/Normal)
3 to 6-year-old
(Frontal/Thick)
7 to 9-year-old
(Lateral/Thin)
8
8
8
8
8
8
8
8
8
8
8-31
8 Specifications
8-32
APR
Number
Imaging
Region
Projection
Direction
95*1
Abdomen
96
Abdomen
Lateral
97
Abdomen
98
Body
Thickness
kV
mAs
Focus Size
58
Small
Thick
95
63
Small
Oblique
Thin
78
80
Small
Abdomen
Oblique
Normal
83
90
Small
99
Abdomen
Oblique
Thick
89
100
Small
100
Waist
Frontal
Thin
68
22
Small
101
Waist
Frontal
Normal
68
25
Small
102
Waist
Frontal
Thick
71
25
Small
103
Waist
Lateral
Thin
82
22
Small
104
Waist
Lateral
Normal
84
25
Small
105
Waist
Lateral
Thick
86
28
Small
106
Waist
Oblique
Thin
71
22
Small
107
Waist
Oblique
Normal
74
25
Small
108
Waist
Oblique
Thick
76
28
Small
109
Leg
Frontal
Thin
63
7.1
Large
110
Leg
Frontal
Normal
63
Large
111
Leg
Frontal
Thick
66
Large
112
Leg
Lateral
Thin
65
7.1
Large
113
Leg
Lateral
Normal
68
7.1
Large
114
Leg
Lateral
Thick
71
7.1
Large
115
Leg
Oblique
Thin
65
Large
116
Leg
Oblique
Normal
65
Large
117
Leg
Oblique
Thick
65
10
Large
118
Foot
Frontal
Thin
58
2.2
Small
119
Foot
Frontal
Normal
58
2.2
Small
120
Foot
Frontal
Thick
61
2.5
Small
121
Foot
Lateral
Thin
57
Small
122
Foot
Lateral
Normal
58
Small
123
Foot
Lateral
Thick
61
Small
124
Foot
Oblique
Thin
55
2.5
Small
125
Foot
Oblique
Normal
58
2.5
Small
10 to 12-year-old
(Lateral/Normal)
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
126
Foot
Oblique
Thick
61
2.8
Small
127
Arm
Frontal
Thin
58
2.8
Small
128
Arm
Frontal
Normal
58
3.2
Small
129
Arm
Frontal
Thick
61
3.2
Small
130
Arm
Lateral
Thin
61
2.8
Small
131
Arm
Lateral
Normal
63
3.2
Small
132
Arm
Lateral
Thick
65
3.6
Small
133
Arm
Oblique
Thin
60
3.2
Small
134
Arm
Oblique
Normal
60
3.6
Small
135
Arm
Oblique
Thick
60
Small
136
Hand
Frontal
Thin
53
0.9
Small
137
Hand
Frontal
Normal
53
Small
138
Hand
Frontal
Thick
56
Small
139
Hand
Lateral
Thin
56
0.9
Small
140
Hand
Lateral
Normal
58
0.9
Small
141
Hand
Lateral
Thick
60
0.9
Small
142
Hand
Oblique
Thin
56
Small
143
Hand
Oblique
Normal
57
Small
144
Hand
Oblique
Thick
57
1.1
Small
*1: The imaging region, projection direction and body thickness displayed on the DR system are not linked to each LED's
illumination status on the X-ray control panel.
8
8
8
8
8
8
8
8
8
CXDI-60C
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
73
Head
Frontal
Thin
64
7.1
Small
74
Head
Frontal
Normal
64
Small
75
Head
Frontal
Thick
66
Small
76
Head
Lateral
Thin
56
7.1
Small
77
Head
Lateral
Normal
58
7.1
Small
78
Head
Lateral
Thick
61
7.1
Small
79
Head
Oblique
Thin
56
Small
80
Head
Oblique
Normal
59
Small
8-33
8
8
8
8
8 Specifications
8-34
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
81
Head
Oblique
Thick
62
Small
82*1
Chest
52
1.1
Large
83*1
Chest
55
1.2
Large
84*1
Chest
57
1.4
Large
85*1
Chest
59
1.4
Large
86*1
Chest
60
1.4
Large
87
Chest
Lateral
Thick
95
Large
88
Chest
Oblique
Thin
87
1.6
Large
89
Chest
Oblique
Normal
90
1.6
Large
90
Chest
Oblique
Thick
93
1.6
Large
91*1
Abdomen
50
1.1
Small
92*1
Abdomen
52
1.2
Small
93*1
Abdomen
55
1.4
Small
94*1
Abdomen
58
1.6
Small
95*1
Abdomen
58
Small
96
Abdomen
Lateral
Thick
95
32
Small
97
Abdomen
Oblique
Thin
78
40
Small
98
Abdomen
Oblique
Normal
83
45
Small
99
Abdomen
Oblique
Thick
89
50
Small
100
Waist
Frontal
Thin
68
11
Small
101
Waist
Frontal
Normal
68
12
Small
102
Waist
Frontal
Thick
71
12
Small
103
Waist
Lateral
Thin
82
11
Small
104
Waist
Lateral
Normal
84
12
Small
105
Waist
Lateral
Thick
86
14
Small
Infant
(Frontal/Thin)
1 and 2-year-old
(Frontal/Normal)
3 to 6-year-old
(Frontal/Thick)
7 to 9-year-old
(Lateral/Thin)
10 to 12-year-old
(Lateral/Normal)
Infant
(Frontal/Thin)
1 and 2-year-old
(Frontal/Normal)
3 to 6-year-old
(Frontal/Thick)
7 to 9-year-old
(Lateral/Thin)
10 to 12-year-old
(Lateral/Normal)
M503-E027
M503-E027
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
106
Waist
Oblique
Thin
71
11
Small
107
Waist
Oblique
Normal
74
12
Small
108
Waist
Oblique
Thick
76
14
Small
109
Leg
Frontal
Thin
63
3.6
Large
110
Leg
Frontal
Normal
63
Large
111
Leg
Frontal
Thick
66
Large
112
Leg
Lateral
Thin
65
3.6
Large
113
Leg
Lateral
Normal
68
3.6
Large
114
Leg
Lateral
Thick
71
3.6
Large
115
Leg
Oblique
Thin
65
Large
116
Leg
Oblique
Normal
65
4.5
Large
117
Leg
Oblique
Thick
65
Large
118
Foot
Frontal
Thin
58
1.1
Small
119
Foot
Frontal
Normal
58
1.1
Small
120
Foot
Frontal
Thick
61
1.2
Small
121
Foot
Lateral
Thin
57
Small
122
Foot
Lateral
Normal
58
Small
123
Foot
Lateral
Thick
61
Small
124
Foot
Oblique
Thin
55
1.2
Small
125
Foot
Oblique
Normal
58
1.2
Small
126
Foot
Oblique
Thick
61
1.4
Small
127
Arm
Frontal
Thin
58
1.4
Small
128
Arm
Frontal
Normal
58
1.6
Small
129
Arm
Frontal
Thick
61
1.6
Small
130
Arm
Lateral
Thin
61
1.4
Small
131
Arm
Lateral
Normal
63
1.6
Small
132
Arm
Lateral
Thick
65
1.8
Small
133
Arm
Oblique
Thin
60
1.6
Small
134
Arm
Oblique
Normal
60
1.8
Small
135
Arm
Oblique
Thick
60
Small
136
Hand
Frontal
Thin
53
0.45
Small
137
Hand
Frontal
Normal
53
0.5
Small
8-35
8
8
8
8
8
8
8
8
8
8
8
8
8
8 Specifications
APR
Number
Imaging
Region
Projection
Direction
Body
Thickness
kV
mAs
Focus Size
138
Hand
Frontal
Thick
56
0.5
Small
139
Hand
Lateral
Thin
56
0.45
Small
140
Hand
Lateral
Normal
58
0.45
Small
141
Hand
Lateral
Thick
60
0.45
Small
142
Hand
Oblique
Thin
56
0.5
Small
143
Hand
Oblique
Normal
57
0.5
Small
144
Hand
Oblique
Thick
57
0.56
Small
*1: The imaging region, projection direction and body thickness displayed on the DR system are not linked to each LED's
illumination status on the X-ray control panel.
8-36
M503-E027
8.7 Labels
8.7
Labels
Locations where the labels are attached are shown as follows.
6
hj
8
28ck
8
h
135fi
klmno
7
h
g
4k
0a
b
8
With FPD upgrade
6
hj
28ck
8
h
135efi
klmno
7
h
g
4k
9
8
8
8
M503-E027
8-37
8 Specifications
J Product Name Plates

1Name plate of MobileArt Evolution High Power Type (32 kW)
2Name plate of collimator R-20C
3Identification label of X-ray control unit MUX-200D-XC (For UL)
8-38
M503-E027
8.7 Labels
4Identification label of high voltage transformer D150MH-40 (For UL)
8
8
8
8
8
8
8
8
8
8
8
8
M503-E027
8-39
8 Specifications
J Warning Labels
5Caution Label A
0Caution Label F
aCaution Label G (Only for grid case)
bCaution Label H (Only for large-sized cassette box)
6Caution Label B
cWarning Label A
dWarning Label B
7Caution Label C
eCaution Label of Breaker
8Caution Label D
fLabel WEEE Mark
9Caution Label E
8-40
M503-E027
8.7 Labels
J Indication Labels
gSmall Movement Switch Label
hBrake Release Switch Label
8
iAdditional Earthing Wire Label
jLabel
8
8
J Other Labels
kCertification Label
8
8
lLabel TUV USA
mEU Representative Label
8
8
nCE Label
oGM Label
8
8
8
8
M503-E027
8-41
8 Specifications
8.7.1
Labeling For X-Ray Tube Unit
t
q
puxy
pvw
z
r
J Name Plates
pName plate of X-ray tube assembly
Name plate of X-ray tube assembly (For UL)
J Warning Labels
qWarning Label (High Voltage)
8-42
rLabel around a radiation gate
M503-E027
8.7 Labels
J Indication Labels
sIndication Label "+" (PLUS)
tIndication Label "-" (MINUS)
8
J Other Labels
uCertification Label
vCE Label
8
wLabel WEEE Mark
xEU Representative Label
8
yGM Label
zLabel TUV USA
8
8
8
8
8
8
M503-E027
8-43
8 Specifications
8.8
8.8.1
Statement of Compliance [For Europe]

Regulatory Information
For Europe:
The product complies with the requirement of the Medical Device Directive 93/42/EEC
Product Name:
MOBILE X-RAY SYSTEM
Model Name:
MOBILE X-RAY SYSTEM MobileArt Evolution High Power Type (32

kW)
Parts Number:
503-70000-XX
Manufacturer:
SHIMADZU CORPORATION
Medical Systems Division
Address:
1, NISHINOKYO-KUWABARACHO,
NAKAGYO-KU, KYOTO, 604-8511, JAPAN
Authorized
SHIMADZU EUROPA GmbH
Representative in EU:
Address:
8.8.2
Albert-Hahn-Strasse 6-10 47269 Duisburg, F.R. Germany
Company's Quality System

The company's Quality System is satisfied with Annex II, Article 3 for 93/42/EEC,
which is certified by TUV Rheinland Product Safety GmbH (Notified under No.0197)
as Registration No: HD 60011592 001
8-44
M503-E027
8.8 Statement of Compliance [For Europe]
8.8.3
International Standards
This unit conforms the following international standards
IEC 60601-1:1988+A1:1991+A2:1995 / EN 60601-1:1990+A1:1993+A2:1995+A3:1996
IEC 60601-1-2:2001+A1:2005 / EN 60601-1-2:2001
IEC 60601-1-3:1994 / EN 60601-1-3:2001
IEC 60601-1-4:2000 Ed.1.1 / EN 60601-1-4:1996+A1:1999
IEC 60601-1-6:2004 / EN 60601-1-6:2004
IEC 60601-2-7:1998 / EN 60601-2-7:1998
IEC 60601-2-28:1993 / EN 60601-2-28:1993
IEC 60601-2-32:1994 / EN 60601-2-32:1994
UL 60601-1:2003 and CAN/CSA C22.2 No.601.IM90
IEC 62220-1:2003 / EN 62220-1:2004
EN ISO 10993-1:2003
EN 980:2003
EN 1041:1998
EN ISO 14971:2000
8
8
8
8
8
8
8
8
8
8
8
8
M503-E027
8-45
8 Specifications
8.9
Manufacturer Information
Manufacturer: SHIMADZU CORPORATION Medical Systems Division
Address: 1, NISHINOKYO-KUWABARACHO, NAKAGYO-KU, KYOTO, 604-8511, JAPAN
8-46
M503-E027
Chapter
FPD Upgrade
J Chapter Contents
9.1
Overview of FPD Upgrade . . . . . . . . . . . . . . . . . . . . . .9-2
9.2
Part Names and Descriptions . . . . . . . . . . . . . . . . . . . .9-3
9.3
Basic Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-12
9.4
Advanced Operation . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
9.5
Optional Features . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-23
9 FPD Upgrade
9.1
Overview of FPD Upgrade

This chapter describes the additional functions, operations and options added by the FPD upgrade.
9.1.1
For information regarding the DR system, refer to the Canon CXDI manual.
Be sure only to use this system after you have fully read and understood all
included documents, including this Operation Manual, attached documentation for
the Canon CXDI-50G, CXDI-50C CXDI-55G, CXDI-55C, CXDI-60G and CXDI60C ("CXDI-50G/50C/55G/55C/60G/60C"), and all warnings, cautions, and notes
contained in the Canon CXDI-50G/50C/55G/55C/60G/60C manual.
CXDI is a registered trademark of Canon Inc.
Features
Immediate Response
A reference image appears on the display in about 3 seconds, allowing on-site image confirmation.
High Throughput
Improves workflow by eliminating the need to prepare a cassette, develop images, or read CR plates,
and using the hospital internal network to send image data to an imager or PACS.
9.1.2
Environmental Conditions
^ Reference "1.3 Environmental Conditions" P.1-4
9-2
M503-E027
9.2 Part Names and Descriptions
9.2
Part Names and Descriptions

X-ray Tube Unit
Column
Arm (P.2-11)
Arm Joint (P.2-11)

Collimator (P.2-8)
Power Supply Panel (P.9-3)

Touch Panel Monitor (P.9-3)
X-ray Control Panel (P.2-6)
Grip Bar (P.2-3)
Hand Switch
(P.2-10)

(P.2-14)
9
9
Imaging Unit (P.9-6)

Storage Case (P.9-10)
9
9.2.1
Power Supply Panel

1
6
7
8
9
9
M503-E027
9-3
9 FPD Upgrade
No.
Name
Function
Key Switch
Battery Indicator
Normally indicates the amount of energy remaining in the battery, but

also indicates charging status during battery recharging.
Power Line Connection

Indicator Lamp
Illuminates when connected to a power outlet.
Charging Lamp
DR Button
USB Connector
^ Reference "Status Indicator Lamp" P.2-5
Turning the key switches system power ON

The key can be removed only in the OFF
or OFF
position.
Blinks when battery is being charged.

Illuminates when charging is complete.
Used to stop travel movement in an emergency situation.
Used to start the DR system.

For DR system operating instructions, refer to the Canon CXDI
manual.
Used to connect external storage media (such as a hard drive or USB
memory unit).
The system is equipped with a color touch panel. The DR system can
be operated by touching the panel.
For DR system operating instructions, refer to the Canon CXDI
manual.
Touch Panel Monitor
Do NOT place or hang objects on the

touch panel.
Doing so could damage the touch panel.
Do NOT press on the panel with a
sharp object, subject it to strong
shocks, or scratch the panel.
Doing so could damage the touch panel.
Ingesting liquid leaked from the touch
panel can be toxic.
9-4
M503-E027
9.2.2
Disposable Wipes Holder
Cylindrical wet tissue containers can be held, with a radius between 120 mm to 150 mm and a height
between 190 mm to 230 mm.
9
9
Disposable Wipes
Holder
9
9
9
The maximum weight capacity is 5 kg.
9
9
9
9
9
9
9
M503-E027
9-5
9 FPD Upgrade
9.2.3
CXDI-50G/50C/55G/55C/60G/60C Imaging Unit

For further details, refer to the Canon CXDI manual.
CXDI-50G/50C
CXDI-55G/55C
CXDI-60G/60C
9-6
M503-E027
9
Treat this precision imaging unit carefully.
Do NOT drop or hit the imaging unit or expose it to large shocks, all of which
could damage the unit or cause it to malfunction.
The imaging unit is equipped with four shock detectors. These detectors are
normally white, but change color if exposed to excessive shock. If even one
shock detector changes color, there is a chance the imaging unit is damaged
or broken. If a shock detector changes color, any damage incurred is not
covered by warranty.
Shock Detectors
9
9
9
CXDI-50G/50C
9
9
9
Shock Detectors
CXDI-55G/55C
9
9
Shock Detectors
CXDI-60G/60C
9
9
9
9
M503-E027
9-7
9 FPD Upgrade
Do NOT pull the cable of the imaging unit.

If the cable catches on something, do NOT pull on the imaging unit. Doing
so can result in cable damage, fire, electric shock, unit damage, or
malfunction.
Do NOT apply any load to the imaging unit that exceed its weight
limit.
Doing so can damage or break the internal sensor of the imaging unit.
<Load limits>
Uniform loads: 150 kg over the entire imaging surface
Point loads: 100 kg / 40 mm dia. area
Be sure to use the imaging unit on a level floor or stand.
If force is applied to the imaging unit at an angle, the internal sensor of the
imaging unit can be damaged or broken.
When handling the imaging unit, be careful not to run over the cable
of the imaging unit with the wheels.
Doing so can damage the cable, cause a fire or electric shock, or damage
the unit.
J Cautions Relating to CXDI-55G/55C/60G/60C
With CXDI-55G/55C/60G/60C, it is possible to turn the imaging unit ON/OFF using the
remote switch.
When performing radiography, press the remote switch to turn it ON.
Remote Switch
9-8
M503-E027
Remove the sensor cable relay connector when replacing the sensor unit, when straightening
the cable to eliminate the torsion, or when the positioning of the sensor unit is not easy with
the sensor cable relay connector attached.
When moving the system, store the sensor cable relay connector in the connector holder.
Connector Holder
Sensor Cable
Relay Connector
9
9
9
9
9
9
When transporting the CXDI-55G/55C/60G/60C, do NOT allow the

sensor cable relay connector to drag on the floor or ground or bump
against anybody or any outside objects or personal property. It is
recommended that the user hold the sensor cable relay connector
while transporting the CXDI-55G/55C/60G/60C.
Failure to do so can cause the sensor cable relay connector to get caught
by, on bump against somebody which may result in injury, or cause
damage to personal property, outside objects and/or the sensor cable
relay connector itself.
When connecting or disconnecting the sensor cable relay connector,
set the power switch of the remote switch to OFF and confirm that
the POWER lamp on both the sensor unit and the remote switch are
off.
The ERROR lamp will light if the sensor cable relay connector is
connected or disconnected while the POWER lamp is lit.
For details about connecting and disconnecting the sensor cable relay
connector, refer to the CXDI Series Operation Manual.
Be sure to hold the sensor cable relay connector by its grip in order
to connect or disconnect it.
Holding the cable to connect or disconnect the sensor cable relay
connector may break the wires inside the cable.
9
9
9
9
9
Do NOT drop the sensor cable relay connector when connecting or

disconnecting it.
You may injure yourself or cause damage to outside objects, personal
property, or the sensor cable relay connector.
M503-E027
9
9-9
9 FPD Upgrade
9.2.4
Storage Case
J One Imaging unit

There are front and rear slots in the storage case.
Rear Slot
Front Slot
CXDI-50G/50C/55G/55C
CXDI-60G/60C
The front slot is used to store the imaging unit. The imaging unit can be stored even with the
grid unit attached.
The rear slot is used to store the grid unit and cassette. If only cassettes are used, up to three
can be inserted.
In the rear slot, the stored grid unit can be attached to and detached from the imaging unit.
Imaging Unit
The grid unit is
attached to
the imaging unit.
Grid Unit
Rear Slot
9-10
M503-E027
9
9
Generating X-rays with a cassette left in the storage case may expose the
film in the cassette.
J Two Imaging Unit

^ Reference "9.5.3 Second FPD Kit" P.9-25
9.2.5
LAN Connector for External Connection

The external connection LAN connector is used for sending obtained image data to external
computers or printers.
Insert the cable into the LAN connector, connect the cable to the external device and transfer data in
DICOM format.
9
9
9
9
LAN Connector
9
9
9
Do NOT connect the LAN connector to external peripherals (such as

printers) not specified by Shimadzu or any devices that do not meet
safety standards.
Doing so could cause unit failure, malfunction, smoke, overheating, electrical
shock, and loss or damage of data.
9
9
M503-E027
9-11
9 FPD Upgrade
9.3
9.3.1
Basic Operation
Starting and Shutting Down the System
^ Reference "3.1 Starting and Shutting Down the System" P.3-2
9.3.2
Aging the X-ray Tube Unit

9.3.3
Moving the System

^ Reference "3.3 Moving the System" P.3-8
9.3.4
Arm Operation
^ Reference "3.4 Arm Operation" P.3-13
9-12
M503-E027
9.3 Basic Operation
9.3.5
J Selecting an Anatomical Program for DR Radiography Mode

Selecting radiography mode in the DR system selects the corresponding anatomical program and
changes the radiography settings to those registered for the program. The corresponding LEDs are
illuminated.
^ Reference For further details on operating the DR system, refer to the Canon CXDI manual.
Anatomical programs cannot be selected from the X-ray control panel during DR
radiography mode.
Pressing the
(FPD/cassette radiography mode button) will not switch the
mode from cassette radiography to DR radiography.
Select a radiography mode from the DR system to switch the mode from the
cassette radiography to the DR radiography. Once done, the corresponding
anatomical program is selected and the radiography parameters are changed to
those registered to that program.
When the
(user settings button) is pressed to switch to the change settings
mode, and then the
(user settings button) is pressed again to return to the
normal mode, the anatomical program changes. From that point, select the
radiography mode using the DR system once again.
9
9
9
9
J Changing to the Cassette Radiography Mode

Switch to the cassette radiography mode on the X-ray control panel.
To switch to the cassette radiography mode, hold down the
for about 2 seconds.
(cassette radiography mode button)
J Selecting an Anatomical Program for Cassette Radiography Mode
^ Reference "Selecting an Anatomical Program for Cassette Radiography Mode" P.3-19
J Manually Setting the Radiography Parameters
9
9
Settings can be changed manually only using the X-ray control panel.
Radiography parameters for the DR system cannot be changed manually.
When manually setting the radiography parameters, refer to the methods described below.
M503-E027
9-13
9 FPD Upgrade
^ Reference "3.5.3 Manually Setting the Radiography Parameters" P.3-20
9.3.6
X-ray Radiography
X-ray tube units must be aged before they can be used. Always age the X-ray
tube unit before radiography.
Inadequate aging may result in the X-ray tube unit discharging during
radiography.
Release the arm lock during radiography.

Radiography is not possible when the system is being moved. To perform
radiography, release the grip bar and inch-mover buttons.
Confirm the DR system READY indicator before attempting radiography.

Attempting radiography before the DR system is ready will result in error F68 and
prevent radiography.
If the DR system exposure time exceeds 1000 msec, the DR system ready time is
extended to about 30 seconds.
J DR Radiography Procedure (Changing to the DR Radiography Mode)
9-14
When using the DR system for a long period of time, connect the power cable to a
power outlet and switch from battery power to outlet power in order to reduce
battery power consumption.
If the system screen is blank after pressing the DR button, and once it is
confirmed that the power cable is not connected to the power outlet, turn both the
key switch and the main circuit breaker to the OFF position, and restart the
system.
Be sure to stop the DR system after use is complete.

If the system is left as is with the DR system operated and the power plug
disconnected from the outlet, the battery will run out. Failure to check may have
an adverse effect on battery life and overall performance.
M503-E027
9.3 Basic Operation
Press the DR button on the upper cover.
The DR system starts up.
Select radiography mode.
* Pressing the
(FPD/cassette radiography mode button) will not switch the mode from
cassette radiography to DR radiography.
Select a radiography mode from the DR system to switch the mode from cassette
radiography to DR radiography. Once done, the corresponding anatomical program is
selected and the radiography parameters are changed to those registered in that program
(except for a part of the radiography methods by CXDI-60G/60C).
When an APR with long-term exposure is selected, the

button) will be illuminated on the control panel.
9
9
(DR long-term exposure
Press the hand switch button to the first level (radiography preparation).
Radiography preparation begins. The status indicator lamp will blink green.
* Radiography preparation cannot start unless the
(standby indicator lamp) is

illuminated. Before pressing the hand switch, confirm that the indicator is illuminated.
During radiography preparation, the collimator lamp will turn off automatically.

to the First Level
9
9
After radiography preparation has finished, the
(radiography ready indicator lamp)
will be illuminated and the status indicator lamp is illuminated green and the collimator
lamp is illuminated again.
* If an X-ray is not radiated within 30 seconds after the radiography preparation is finished,
the preparation will be automatically cancelled. To prepare for radiography again, release
the hand switch from the state pressed to the first level.
9
9
To illuminate the collimator lamp again after the radiography preparation is finished, see
"4.1 User Settings" P.4-2.
Confirm that the DR system is READY before attempting radiography. Attempting
radiography before the DR system is ready will result in error F68 and prevent radiography.
If error F68 appears, cancel the error by confirming the READY indicator on the DR system
touch panel monitor and then pressing the FPD radiography selection button.
Long-term exposure extends the DR system READY time to about 30 seconds.
9
M503-E027
9-15
9 FPD Upgrade
After confirming the DR system READY indicator, press the hand switch
button to the second level (X-ray exposure).
Pressing the button starts X-ray exposure.
During X-ray exposure the
(X-ray irradiation indicator lamp) is illuminated, a sound
is emitted, and the status indicator lamp will be illuminated orange.
* The sound volume during X-ray exposure can be made louder.


to the Second Level
After X-ray exposure, the [kV] and [mAs] displays will blink for 5 seconds.
The status indicator lamp will blink until the battery has recharged.
* During radiography the hand switch (first and second levels) must be continuously and fully
depressed until the exposure finishes. If the switch is released before completion of the
exposure, the exposure will be terminated prematurely. In this case, the film may not be
clear due to insufficient X-ray exposure.
After performing radiography, another image cannot be taken until the battery is recharged.
Wait until the
(standby indicator lamp) is illuminated before performing any operation.
Depending on the radiography parameters, this may require 1 minute or more.
When repeating radiography preparation, release the hand switch (first and second levels)
once.
9-16
M503-E027
9.3 Basic Operation
Confirm the reference image.

After exposure, a reference image will appear on the touch panel monitor. Use the monitor
to check for blurs caused by patient movement.
9
9
The touch panel monitor is not designed for diagnostic use. Displayed images are
for reference use only.
The kV and mAs displays may differ from the radiography parameters displayed
on the touch panel monitor.
The system can save a maximum of 3500 images. If this number is exceeded, the
system automatically deletes excess images, starting from the oldest image (all
images taken in an examination are deleted together).
After DR radiography is completed, press the DR shutdown button on the

touch panel monitor.
The DR system shuts down.
9
9
9
9
If a DR system malfunction occurs, such as not responding, after confirming that

the power cable is not connected to a power outlet, turn the key switch and the
main circuit breaker to OFF, and stop the DR system.
If the DR system is not shut down using the correct procedure, an error will be
displayed on the DR system monitor when the DR system is started up next time.
For further details, refer to the Canon CXDI manual.
9
9
9
J Transferring Images to an External Printer or PACS System
9
Do NOT connect any DICOM printer, workstation, PACS, or other
peripheral device that does not meet safety standards, to the external
LAN connector.
Doing so could cause unit failure, malfunction, smoke, overheating, electric

shock, or loss or damage of data.
Images stored to the system can be output to a DICOM printer, workstation, or PACS.
1
M503-E027
Insert the cable to the external LAN connector at the bottom of the grip bar
and connect it to the printer or network.
9-17
9 FPD Upgrade
Output the image from the DR system according to the Canon CXDI
manual.
^ Reference For further details about the printer or other peripheral units,
refer to the corresponding instruction manual.
J Saving Images to External Media
Do NOT connect any peripheral device to the USB connector that does
not meet IEC 60950-1, or any other safety standards equivalent to IEC
60950-1.
Doing so could cause unit failure, malfunction, smoke, overheating, electric
shock, or data loss or damage.
Connect a hard drive, USB memory device, or other external storage

media to the USB connector on the upper cover.
Save the image to the external media as instructed in the Canon CXDI
manual.
Press the [Eject Media] button on the DR system [Examination Image List]
to remove the media.
Connect the media to a printer, workstation, or other unit and output the
image.
^ Reference For further details about external storage media (such as USB memory device) or
peripherals (such as printers), refer to the manual for that media/device.
J Cassette Radiography Procedure

^ Reference "3.6.1 Cassette Radiography Procedure" P.3-22
9-18
M503-E027
9.4 Advanced Operation
9.4
9.4.1
Advanced Operation
Registering Anatomical Programs
In the anatomical program, a total of 72 types (8 imaging portions x 3 directions x 3 body

thicknesses) can be registered for FPD and cassette radiography respectively.
The following radiography parameters can be registered in the anatomical programs.
^ Reference "2.4 X-Ray Control Panel" P.2-6
J Registration Procedure for DR Radiography
When registering the anatomical programs for DR radiography, make sure the
anatomical code registered for the DR radiography mode matches the anatomical
program number registered for DR radiography.
For further details about editing the DR radiography mode, refer to the Canon
CXDI manual.
For anatomical codes specified in DR radiography modes, see "8.6 Anatomical
Program" P.8-23.
If using anatomical programs for DR radiography, register radiography parameters

that result in exposure times less than the maximum permitted by the DR system.
The maximum exposure time for the DR system is initially set to 1000 msec. It is
possible, however, to extend this to 3000 msec by switching to the DR long-term
exposure mode. If the DR system exposure time exceeds 1000 msec, the DR
system READY time is extended to about 30 seconds.
Settings on DR System
Specify radiography parameters for the DR radiography mode.

^ Reference Refer to the Cannon CXDI manual for further details about editing the DR
radiography mode.
Specify an anatomical program number that matches the anatomical code

specified for the DR radiography mode.
Register specified radiography parameters.
9
9
M503-E027
9-19
9 FPD Upgrade
Select the DR radiography mode

Check that the anatomical program that corresponds to that on the X-ray control panel has
been selected.
Settings on Main Unit
On the X-ray control panel, specify the radiography parameters and focal
size to be registered.
Specify the radiography parameters and focal size specified for DR radiography mode to
the anatomical program.
^ Reference "3.5.3 Manually Setting the Radiography Parameters" P.3-20
If radiography parameters cannot be set, it means that the exposure time exceeds
1000 msec. Change the anatomical program to the DR long-term exposure mode and
specify the radiography parameters.
^ Reference "Procedure for Changing to DR Long-Term Exposure Mode" P.9-20
If reducing exposure time from more than 1000 msec to less than 1000 msec, change
the anatomical program from DR long-term exposure mode to DR radiography mode
before registering radiography parameters.
^ Reference "Changing from DR Long-Term Exposure Mode to DR Radiography Mode"
P.9-21
Press the
(registration button) for about 3 seconds.
Keep pressing the

(registration button) until [aPr set] appears on the X-ray control
panel, which indicates that the anatomical program has been registered.
During DR long-term exposure mode, the
illuminated.
(DR long-term exposure button) will be
When registering anatomical programs, do not release the registration button until
[aPr set] appears on the X-ray control panel.
Procedure for Changing to DR Long-Term Exposure Mode
9-20
Press the
(DR long-term exposure button).
The
(DR long-term exposure button) blinks.
Press the
M503-E027
9.4 Advanced Operation
Hold down the

(registration button) for about 3 seconds until [aPr set] appears
on the X-ray control panel to register the DR long-term exposure mode.
When the DR long-term exposure mode is registered, the
(DR long-term
exposure button) will illuminate.
Specify the radiography parameters to be registered to the DR long-term exposure

mode.
Changing from DR Long-Term Exposure Mode to DR Radiography Mode
Set radiography parameters to below 1000 msec.
Press the
(DR long-term exposure button) when it is illuminated.
The
(DR long-term exposure button) turns OFF.
9
9
Make sure that the imaging region, projection direction, body thickness correction, and
radiography parameters are specified as intended.
J Registration Procedure for Cassette Radiography

^ Reference "Registration Procedure for Cassette Radiography" P.4-14
9
9
9
9
9
9
9
9
M503-E027
9-21
9 FPD Upgrade
9.4.2
Deleting Unused Anatomical Programs

Anatomical programs not normally used, can be deleted.
Once an anatomical program is deleted it can no longer be used for radiography, even if it is selected.
If a deleted anatomical program is selected, [aPr set] appears on the X-ray control panel.
J Deleting Unused Anatomical Programs
Select the anatomical program to delete.

Select the unused imaging region, projection direction, and body thickness correction.
Hold down the

about 3 seconds.
(registration button) and press mAs [+] button for
Keep pressing the

(registration button) and mAs [+] button until [del ete] appears on
the X-ray control panel, which indicates the anatomical program has been deleted.
[_ _ _ _ _ _] appears on the X-ray control panel.
When deleting an anatomical program, do not release the registration button and
mAs [+] button until [del ete] appears on the X-ray control panel.
After deleting an anatomical program, change the correspondence between the

anatomical program number and the anatomical code specified for DR
radiography.
J How to Use the Deleted Anatomical Program

^ Reference "Registration Procedure for Cassette Radiography" P.4-14
9-22
M503-E027
9.5 Optional Features
9.5
Optional Features
In addition to the standard options, the following options can be added.
Grid Unit
Wireless LAN Option
Second FPD Kit
FPD Bag
9
9
9
After FPD upgrade, the grid case and the large-sized cassette box cannot be
attached.
9.5.1
Grid Unit
The optional grid unit can be attached to the FPD imaging unit.
When the grid unit is not being used, store it in the rear slot of the storage case.
^ Reference For detailed information about attaching and detaching the grid unit, refer to the Canon CXDI
manual.
CXDI-50G/50C
9
9
CXDI-55G/55C
9
9
CXDI-60G/60C
9
9
M503-E027
9-23
9 FPD Upgrade
9.5.2
Wireless LAN Option

By attaching a commercial wireless LAN adapter (USB connection-type), images stored on the
system can be transferred through a wireless LAN network to a DICOM printer, workstation, PACS,
or other external device.
Wireless LAN Adapter
J Using a Wireless LAN Adapter

Connect to the wireless LAN network.
1
2
Output images using the DR system, as described in the Canon CXDI

manual.
Refer to the manual that comes with the wireless LAN adapter for further
information.
When connected to both wired and wireless LAN networks, the wired network
takes priority.
J Wireless LAN Adapter Specifications

Item
9-24
Description
Connection
USB 2.0
Standard
IEEE 802. 11g, IEEE 802. 11b
Frequency Range
2.4 GHz range
Bandwidth
2412 to 2472 MHz
Other
No auto-install function
Recommended Product
Netgear WG111 (functionality verified by Shimadzu)
M503-E027
9.5.3
Second FPD Kit
2 imaging units are available by this kit. Imaging units are alternated by detachable the sensor cable
relay connector.
J Using the Sensor Unit Attach/Detach Function
1
2
3
4
Turn OFF the remote switch.
Disconnect the sensor cable relay connector from the sensor unit.
Connect the sensor cable relay connector to the sensor unit.
Turn ON the remote switch.

^ Reference For details about connecting and disconnecting the sensor cable relay
Remove the sensor cable relay connector when replacing the sensor unit, when straightening
the cable to eliminate the torsion, or when the positioning of the sensor unit is not easy with
the sensor cable relay connector attached.
When moving the system, store the sensor cable relay connector in the connector holder.
Connector Holder
Sensor Cable
Relay Connector
9
9
9
9
9
9
9
9
9
M503-E027
9-25
9 FPD Upgrade
Store the sensor cable relay connector of the unused sensor unit in the connector holder.
Connector Holder
When transporting the CXDI-55G/55C/60G/60C, do NOT allow the

sensor cable relay connector to drag on the floor or ground or bump
against anybody or any outside objects or personal property. It is
recommended that the user hold the sensor cable relay connector
while transporting the CXDI-55G/55C/60G/60C.
Failure to do so can cause the sensor cable relay connector to get caught
by, or bump against somebody which may result in injury, or cause
damage to personal property, outside objects and/or the sensor cable
relay connector itself.
When connecting or disconnecting the sensor cable relay connector,
set the power switch of the remote switch to OFF and confirm that
the POWER lamp on both the sensor unit and the remote switch are
off.
The ERROR lamp will light if the sensor cable relay connector is
connected or disconnected while the POWER lamp is lit.
For details about connecting and disconnecting the sensor cable relay
Be sure to hold the sensor cable relay connector by its grip in order
to connect or disconnect it.
Holding the cable to connect or disconnect the sensor cable relay
connector may break the wires inside the cable.
Do NOT drop the sensor cable relay connector when connecting or
disconnecting it.
You may injure yourself or cause damage to outside objects, personal
property, or the sensor cable relay connector.
9-26
M503-E027
J Storage case
There are front, middle and rear slots in the storage case for Second FPD kit.
Rear Slot
Middle Slot
Front Slot
9
9
The front slot is used to store the CXDI-55G/55C imaging unit. The imaging unit can be
stored even with the grid unit attached.
The middle slot is used to store the CXDI-60G/60C imaging unit. The imaging unit can be
stored even with the grid unit attached.
The rear slot is used to store the grid unit and cassette.
In the rear slot, the stored grid unit can be attached to and detached from the imaging unit.
9
9
9
Generating X-rays with a cassette left in the storage case may expose the
film in the cassette.
9
9
9
9
9
9
M503-E027
9-27
9 FPD Upgrade
9.5.4
FPD Bag
This bag allows the imaging unit to slide smoothly.
Put the bag over the imaging unit.
9-28
M503-E027
Appendix
10
Appendix
Check List for Trouble

Fill following blanks and contact the Shimadzu service representative.
Hospital :
Phone :
FAX :
Serial Number:
Date of Installation:
Item
Check
Someone injured
When did the trouble occur?
Is there a sign of the trouble?
Is there a power failure or thunderbolt when the trouble
occurred?
The device has been watered?
The device has been given an impact?
The number of patients a day with the device?
When is the last periodic inspection?
App-2
M503-E027
Appendix
10
Safety Check Registry
10
Name
Phone
Extension number
10
Hospital
FAX
Address
Room number
10
Name
Device
Serial number
10
Date of installation
Affiliation
Instructor
Phone
10
FAX
Date
Description
This device's
maintenance and
operation staff
Instructor
Signature
Signature
10
10
10
10
10
M503-E027
At the time of installation or when changing the designated operator, the Shimadzu service
representative will explain the safety instructions described in this manual to the maintenance
and operation staff, and record the information.
This manual is important. We request all maintenance personnel to keep it in a safe place
close to the device.
App-3
10
10
Index
Index
A
Collimator lamp control setting.................................. 4-2

Column ................................................................... 9-3
Acc......................................................................... 4-5
CPU backup battery................................................ 4-18
Acceleration setting.................................................. 4-2
Current-time product...............................................3-19
Additional hand switch ........................................... 5-16
Current-time product buttons ..................................... 2-7
Additional protective grounding wire....................... 2-15
CXDI-50C ...............................................................9-6
Additional radiography function .............................. 3-25
CXDI-50G...............................................................9-6
Aging ..................................................................... 3-6
CXDI-55C ...............................................................9-6
All Free button ............................................... 2-8, 2-11
CXDI-55G...............................................................9-6
Anatomical code .................................................... 9-19
CXDI-60C ...............................................................9-6
Anatomical program............................... 3-19, 1-3, 4-14
CXDI-60G...............................................................9-6
Anatomical program number.......................... 8-23, 9-19

APO ....................................................................... 4-6
APR ..................................... 1-3, 3-19, 4-8, 8-23, 8-26

aPr.......................................................................... 4-8
Disposable wipes holder............................................ 9-5
APR settings at startup ............................................. 4-2
Distance indicator................................................... 5-11
Apron hanger......................................................... 2-12
Dose area product meter............................................ 5-7
Arm ............................................................... 2-11, 9-3
Dose calculation unit ................................................ 5-9
Arm joint ....................................................... 2-11, 9-3
DR button ................................................................ 9-4
Arm lock release button.......................................... 2-11
DR long-term exposure button ...................................2-6
Arm lock release buttons .......................................... 2-8
DR long-term exposure mode .................................. 9-20
Arm lock release lever............................................ 2-11
DR radiography mode............................................. 9-13
at OFF .................................................................... 3-5
DR system .................................................... 9-13, 9-14
Auto-power-OFF function ........................................ 3-5

Auto-power-off time setting...................................... 4-2
E
Emergency brake release battery ..............................4-18
Emergency brake release button........................ 2-3, 4-17
bAC........................................................................ 4-6
Emergency stop button..............................2-4, 3-12, 9-4
Backward power-assist setting................................... 4-2

Battery.................................................................. 3-26
Battery indicator ............................................... 2-4, 9-4
Body thickness selection buttons ............................... 2-7
bon ......................................................................... 4-7
Brake release bar ..................................................... 2-3
Buzzer setting.......................................................... 4-2
F
Focus mode button ................................................... 2-6
FPD bag ................................................................9-28
FPD/Cassette radiography mode button ...................... 2-6
Front slot ............................................................... 9-27
C
Cassette radiography mode ............................ 3-19, 9-13
Changing the grip bar height ................................... 5-14
Charging ............................................................... 3-27
Charging lamp .................................................. 2-4, 9-4
Check List for Trouble ........................................... 10-2
Collimator........................................................ 2-8, 9-3
Grid unit ................................................................9-23

Grip bar ............................................................ 2-3, 9-3
Grounding cable .......................................................7-5
H
Hand switch .................................................... 2-10, 9-3
Collimator lamp button............................. 2-6, 2-8, 4-13
M503-E027
Index-1
Index
Imaging region selection buttons................................ 2-7
PACS ....................................................................9-17
Imaging unit ..................................................... 9-3, 9-6
PAS.........................................................................4-4
Inch-mover buttons.......................................... 2-8, 3-10
Password................................................................5-12
Irradiation field ...................................................... 3-17
Periodic replacement parts .........................................7-8
Irradiation field adjustment knobs .............................. 2-8
Personal ID setting....................................................4-2
Pid...........................................................................4-4
Positioning .............................................................3-15
Key switch........................................................ 2-4, 9-4

Keyless entry ......................................................... 5-12
kV display ............................................................... 2-7
Power cable............................................................2-13
Power line connection indicator lamp ..................2-4, 9-4
Power supply panel ............................................2-4, 9-3
Power-assist setting...................................................4-2
Projection direction selection buttons..........................2-7
Protective screen.......................................................5-5
LAN connector for external connection .................... 9-11

LAP ........................................................................ 4-7
Large focus............................................................ 8-19
Locking the arm ..................................................... 3-13
Low-battery mode .................................................. 3-24
Low-speed travel mode............................................. 3-9
Luminous hand switch ............................................ 5-15
R
Radiography parameters .................................3-19, 8-19
Radiography preparation button ...............................2-10
Radiography ready indicator lamp ..............................2-6
READY .................................................................9-14
Rear slot ................................................................9-27
Registration button....................................................2-7
Releasing the brake in emergency.............................4-17
Main circuit breaker ........................................ 2-14, 9-3
Remaining battery charge ..........................................3-2
Malfunction indicator lamp ................................ 2-6, 6-4
Remote control receiver.............................................5-3
mAs ...................................................................... 3-19
Remote controller .....................................................5-2
mAs display............................................................. 2-7
Remote controller button ...........................................2-6
Middle slot ............................................................ 9-27
Remote switch ..........................................................9-9
Motor.................................................................... 4-18
Replacement time display ........................................4-18
Normal travel mode.................................................. 3-9
Safety check registry ...............................................10-3
Notification function............................................... 4-18
Second FPD kit.......................................................9-25

Sensor cable relay connector ......................................9-9
Symbols
Small focus ............................................................8-20

Snd..........................................................................4-9
Numeric Delete Button ........................................... 5-12
sound emitted during system travel.............................4-9
Numeric keypad ..................................................... 5-12
sound emitted during X-ray exposure..........................4-9

sound emitted when radiography preparation
is finished ................................................................4-9
Obstruction detector ............................................... 3-11
Standby indicator lamp..............................................2-6
Obstruction detector canceling function.................... 3-11
Status indicator lamp...................................1-3, 2-4, 9-4
Operation sound ..................................................... 4-12
stc ...........................................................................4-5
Operation sound setting ............................................ 4-2
Steer control setting ..................................................4-2

Storage case ....................................................9-3, 9-10
Index-2
M503-E027
Index
1
T
Tape measure ................................................. 2-8, 3-17

Top plate................................................................. 7-3
Touch panel monitor ......................................... 9-3, 9-4
Transmission status indicator .................................... 5-2
Travelling warning sound ......................................... 2-6

Tube voltage.......................................................... 3-19
Tube voltage buttons ................................................ 2-7
U
U01 ...................................................................... 4-18
U02 ...................................................................... 4-18
U03 ...................................................................... 4-18
U04 ...................................................................... 4-18

U05 ...................................................................... 4-18
USB connector ........................................................ 9-4
User settings button.................................................. 2-7
User settings mode ................................................... 4-3
Warning indicator lamp ..................................... 2-6, 6-2

Wire rope ................................................................ 7-5
Wireless LAN option ............................................. 9-24
X
X-ray control panel ........................................... 2-6, 9-3
X-ray exposure button ............................................ 2-10
X-ray irradiation indicator lamp ................................ 2-6
X-ray tube unit ........................................ 3-6, 4-18, 9-3
1
1
1
1
M503-E027
Index-3

Operation Manual M503E027A

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Operation Manual M503E027A

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Manual No.

MOBILE X-RAY SYSTEM

Read this manual carefully to ensure appropriate use,

About the symbols appearing in this operation

States information which helps to use the system correctly.

Provides reference information.

Added "CXDI-55G/55C and 60C", "8.9 Manufacturer Information", "9 FPD

X-ray Tube Unit

Be sure to keep this manual nearby for future reference.

2009 Shimadzu Corporation. All rights reserved.

"Operating Precautions (for Both Safety and the Prevention of

Only an experienced technician should operate the equipment.

When installing the equipment, pay attention to the following items:

Before operating the equipment, pay attention to the following items:

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

While operating the equipment, pay attention to the following items:

After operating the equipment, pay attention to the following items:

Keep it away from water.

Store it away from potential causes of problems such as abnormal

(iii) During transportation and storage of the equipment, avoid tilting,

Do not modify any part of the equipment.

(1) The equipment and its parts should be periodically checked.

Concerning other items, operate properly according to the operation

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

The responsibility for management of use and maintenance of medical

NEVER MODIFY THE EQUIPMENT!

PERFORM PERIODIC INSPECTION!

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

Repair and maintenance of equipment can only be performed by

If the operator has no experience in operating the equipment, be sure

In order to operate the equipment safely, an explanation of the operation

^ Reference "1.5 Operator Profile" P.1-7

Be sure to Read the Safety Items to Prevent from Explosion or

Do NOT use the system in an atmosphere containing combustible gas.

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

Do NOT use disinfectant sprays that are flammable or could cause an

This equipment has no protection against exposure to liquids. Do NOT

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

Collision and Entanglement

Charge the battery in a well-ventilated room. Do NOT cover the system

Cautions on Use and Storage

No explosive or corrosive gases

700 to 1060 hPa

Note also that there must be no sudden changes in temperature or

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

Cautions on Cleaning and Disinfection

Clean and disinfect the system.

Do NOT apply disinfectant directly, or spray it, onto the system.

Do NOT use an organic solvent.

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

Cautions Relating to Cellular Telephones

Do NOT bring cellular telephones or related devices into the

Cautions on the Compatibility of Electromagnetic Fields

MobileArt Evolution High Power Type (32 kW) needs special

^ Reference "8.1 Environmental Conditions of EMC (Electro-Magnetic Compatibility)" P.8-2

Check that the electromagnetic fields are compatible.

^ Reference "8.1 Environmental Conditions of EMC (Electro-Magnetic Compatibility)" P.8-2

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

Do NOT allow operation of this apparatus by any person other than

Be aware of the potential for X-ray irradiation.

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL

^ Reference "3.2 Aging the X-Ray Tube Unit" P.3-6

Avoid unnecessary standby situations.

MobileArt Evolution High Power Type (32 kW) OPERATION MANUAL