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GE Healthcare
Service Manual
All rights reserved. General Electric Company reserves the right to make changes in
specifications and features shown herein, or discontinue the product described at
any time without notice or obligation. Contact your GE Representative for the most
current information. Panda is a trademark owned by Datex-Ohmeda, Inc. GE and
GE Monogram are trademarks of General Electric Company. All other company and
product names mentioned may be trademarks of the companies with which they
are associated.
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Table of Contents
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Section 2 Checkout and Installation...............................................................................................2-1
2.1 Warmer Maintenance Schedule................................................................................................................ 2-1
2.1.1 Operator maintenance.................................................................................................................... 2-1
2.1.2 After each patient use .................................................................................................................... 2-1
2.1.3 Service maintenance ...................................................................................................................... 2-1
2.1.4 Annually.................................................................................................................................................. 2-1
2.1.5 Every Two Years.................................................................................................................................. 2-1
2.1.6 Service tools ........................................................................................................................................ 2-2
2.2 Installation and Service Checkout Procedures................................................................................... 2-2
2.2.1 Mechanical checks............................................................................................................................ 2-2
2.2.2 Controller checks .............................................................................................................................. 2-3
2.3 Electrical Safety Tests..................................................................................................................................... 2-3
2.3.1 Ground Resistance Check.............................................................................................................. 2-3
2.3.2 Earth Leakage and Chassis Leakage current....................................................................... 2-4
2.3.3 Patient Lead Leakage Current .................................................................................................... 2-4
Section 3 Calibration.............................................................................................................................3-1
3.1 Scale Calibration............................................................................................................................................... 3-1
Section 4 Troubleshooting..................................................................................................................4-1
4.1 Service Mode...................................................................................................................................................... 4-1
4.1.1 Unit Specific Information . ............................................................................................................. 4-1
4.1.2 Operator Settings............................................................................................................................... 4-2
4.1.3 Calibration ............................................................................................................................................ 4-2
4.1.4 Date/Time . ........................................................................................................................................... 4-2
4.1.5 Diagnostics............................................................................................................................................ 4-3
4.1.6 Diagnostics using serial port........................................................................................................ 4-4
4.1.7 File Capture........................................................................................................................................... 4-4
4.2 Test points............................................................................................................................................................ 4-6
4.3 Troubleshooting Tables................................................................................................................................. 4-8
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5.2.3 Lithium ion battery replacement (Figures 5-3, 5-4 and 6-14 ....................................... 5-6
5.2.4 Touch panel or LCD assembly (Figures 5-4 and 5-5)........................................................ 5-7
5.2.5 Observation light dimmer control (Figure 5-5)..................................................................... 5-8
5.2.6 Standby Switch replacement (Figure 5-5)............................................................................... 5-8
5.2.7 Outlet panel repairs (Figures 5-4 & 5-6)................................................................................... 5-8
5.2.8 Maneuvering handle......................................................................................................................... 5-9
5.3 Probe Panel Housing Repairs...................................................................................................................... 5-9
5.3.1 Probe Panel Housing Disassembly (Figure 5-7).................................................................... 5-9
5.3.2 SpO2 Interface Board Replacement (Figure 5-7)................................................................5-10
5.3.3 SpO2 Connector/Flex Circuit Replacement (Figure 5-7)..................................................5-10
5.3.4 Scale Connector Replacement (Figure 5-7)..........................................................................5-11
5.3.5 Patient Probe Connector Replacement (Figure 5-7)........................................................5-11
5.4 Lower Unit repairs..........................................................................................................................................5-11
5.4.1 Removing the bed (Figures 5-8 and 5-9)...............................................................................5-11
5.4.2 Elevating column replacement (Figure 5-10.......................................................................5-13
5.4.3 Adjusting manual bed height units..........................................................................................5-13
5.5.4 Footswitches (Figure 5-10)..........................................................................................................5-14
5.5.5 Caster Replacement (Figure 5-10)............................................................................................5-14
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Appendix BElectromagnetic Compatibility................................................................................. B-1
Electromagnetic compatibility (EMC) guidance......................................................................................... B-1
Manufacturers guidance and declaration regarding electronic emissions................................ B-2
Manufacturers guidance and declaration regarding electromagnetic immunity................... B-3
International Electronic Commission (IEC) guidance and manufacturers declaration regarding
electronic immunity................................................................................................................................................ B-4
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The intended users for this service manual are identified in the Important Safety Information section on
page ix.
Important Safety Information provides important safety information for the safety of the patients,
care providers and biomedical engineering service personnel.
Section 1 - Functional Description describes functions and identifies the sub-assemblies of the
Panda iRes and Giraffe Warmers, including the optional resuscitation and oximetry equipment.
Section 2 - Checkout and Installation describes the procedures to set up and check out the Panda
iRes and Giraffe Warmers prior to use.
Section 5 - Repair Procedures provides the procedures for the repair of the units sub-assemblies.
Section 6 - Illustrated Parts provides expanded diagrams of the units sub-assemblies and associ-
ated part numbers.
Appendix B - Electromagnetic Compatibility (EMC) provides information on the Panda iRes and
Giraffe Warmers electromagnetic emissions and the electronic environment that is compatible with
the use and operation of the warmers.
Appendix C - Conforming with Standards and Directives provides information on the European
Council Directive and the disposal of electrical/electronic equipment.
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References
References to other manuals pertaining to the Panda iRes and Giraffe Warmers are:
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Complete the Checkout Procedures section in the Operation and Maintenance manual before putting the
unit into operation. If the warmer fails any portion of the checkout procedure it must be removed from use
and repaired.
Always disconnect the power before performing service or maintenance procedures detailed in this manual.
Apply power only if you are specifically instructed to do so as part of the procedure. Thoroughly air dry the
warmer after cleaning it with flammable agents. Small amounts of flammable agents, such as ether, alcohol
or similar cleaning solvents left in the warmer can cause a fire.
Only competent individuals trained in the repair of this equipment should attempt to service it as detailed in
this manual.
Detailed information for more extensive repairs is included in the service manual solely for the convenience
of users having proper knowledge, tools and test equipment, and for service representatives trained by GE
Healthcare.
The information contained in this service manual pertains only to those models of products which are
marketed by GE Healthcare as of the effective date of this manual or the latest revision thereof. This service
manual was prepared for exclusive use by GE Healthcare service personnel in light of their training and expe-
rience as well as the availability to them of parts, proper tools and test equipment. Consequently, GE Health-
care provides this service manual to its customers purely as a business convenience and for the customers
general information only without warranty of the results with respect to any application of such information.
Furthermore, because of the wide variety of circumstances under which maintenance and repair activities
may be performed and the unique nature of each individuals own experience, capacity, and qualifications,
the fact that a customer has received such information from GE Healthcare does not imply in anyway that
GE Healthcare deems said individual to be qualified to perform any such maintenance or repair service.
Moreover, it should not be assumed that every acceptable test and safety procedure or method, precaution,
tool, equipment or device is referred to within, or that abnormal or unusual circumstances, may not warrant
or suggest different or additional procedures or requirements. This manual is subject to periodic review, up-
date and revision. Customers are cautioned to obtain and consult the latest revision before undertaking any
service of the equipment.
This static control precaution symbol appears throughout this manual. When this symbol appears next to a
procedure in this manual, static control precautions MUST be observed. Use the static control work station
(Stock No. 0175-2311-000) to help ensure that static charges are safely conducted to ground and not
through static sensitive devices.
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This section introduces the format in which the various types of warnings, cautions, static control
precautions and information notes used in this service manual are displayed to alert you to possible safety
hazards and to provide you with additional information.
warning:
A Warning statement is used when the possibility of injury to the patient or the operator exists.
Caution:
A Caution statement is used when the possibility of damage to the equipment exists.
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This section identifies general warnings, cautions and notes associated with the use and servicing of the
Panda iRes and Giraffe Warmers.
warning:
Do not use the warmer in the presence of flammable anesthetics; an explosion hazard exists under
these conditions.
warning:
Thoroughly air dry the warmer after cleaning it with flammable agents. Small amounts of flamma-
ble agents, such as ether, alcohol or similar cleaning solvents left in the incubator can cause a fire.
warning:
Do not attempt to adjust the fixed base while a patient is in the bed. After adjustments to the fixed
base height have been made, ensure the fixed base is locked in place before placing a patient in the
bed.
warning:
Always connect the warmer directly to a hospital grade wall outlet. Connecting to a power strip or
another piece of equipment may result in shock hazard.
warning:
Do not service, program or calibrate the warmer with the patient in the bed.
warning:
Do not lean against side of warmer. Leaning against the side of the warmer may cause it to tip
over.
warning:
Bed-to-heater spacing less than approximately 85 cm will result in incorrect operation and may
adversely affect the patients condition.
Caution:
Servicing of this product in accordance with this service manual should never be undertaken in the
absence of proper tools, test equipment and the most recent revision to this service manual which
is clearly and thoroughly understood.
Caution:
Always disconnect the power before performing service or maintenance procedures detailed in this
manual. Apply power only if you are specifically instructed to do so as part of the procedure.
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Caution:
Technical competence required to service the warmers; the procedures described in this service
manual should be performed by trained and authorized personnel only. Maintenance should only
be undertaken by competent individuals who have a general knowledge of and experience with de-
vices of this nature. No repairs should ever be undertaken or attempted by anyone not having such
qualifications. Genuine replacement parts manufactured or sold by GE Healthcare must be used for
all repairs. Read completely through each step in every procedure before starting the procedure;
any exceptions may result in a failure to properly and safely complete the attempted procedure.
CAUTION:
U.S. Federal law restricts this device to sale by, or on order of, a licensed medical practitioner.
CAUTION:
This device is for professional use only, by trained clinicians.
NOTE: Ranges listed in this supplement manual represent the operational ranges of the equip-
ment. The gauge ranges may exceed operational ranges.
NOTE: Additional copies of this manual are available on request from the GE Healthcare office
listed on the inside back cover of this manual.
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Symbols
This section identifies the symbols that are displayed on the Panda iRes and Giraffe Warmers:
Symbol Description
Type BF Equipment
Alternating Current
Alarm Silence
Catalog Number
Serial Number
Manufacturer
Do not reuse
Help menu
Patient temperature
Observation light
Scale
Date of manufacture
Increase/decrease, up/down
This symbol indicates that the waste of electrical and electronic equipment
must not be disposed as an unsorted municipal waste and must be collected
separately. Please contact an authorized representative of the manufacturer
for information concerning the decommissioning of your equipment.
Equipment shall be used only by qualified, trained medical personnel.
For professional use only
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Section 1
Functional Description
1.1 Introduction
The GE Healthcare Panda iRes and Giraffe Warmers are devices with a radiant heating source
intended to maintain the thermal balance of an infant patient by direct radiation of energy in the
infrared region of the electromagnetic spectrum.
Radiant heat from an infrared heat source is focused onto the bed to warm the patient. The operator
may select either the heater power (manual mode) or skin temperature (baby mode) control method.
Depending on the control method selected, the heater is either regulated at the operator selected
power level or the heater output is modulated to maintain the patients temperature at the value
selected by the operator.
The Giraffe model is intended for use in a neonatal intensive care unit. It features a mattress which
can be rotated as needed by the operator to gain better access to the patient. Also included are gen-
eral observation lights and a procedure light.
The procedure light is mounted on a ball joint so that it can be directed where needed on the bed
surface.
The Panda iRes model is intended for use in a labor and delivery unit. It also includes the same gen-
eral observation lights as the Giraffe Warmer, but the procedure light is optional.
Both units feature the same heater head to house the radiant heater. Due to the small size of the
heater reflector and its compound elliptical shape, designed specifically for this product, the heater
head is very compact compared with other warmers currently on the market. This compact size
limits the area the heater head occupies over the bed surface. By leaving the area over the bed clear,
the caregiver can observe and treat the patient unobstructed. Additionally, this open area allows the
head of an X-ray machine to be placed over the patient without moving the heater head or patient.
Both units also feature optional integrated SpO2 and Resuscitation Modules. The SpO2 option allows
the caregiver to monitor the patients blood oxygen level, while the optional Resuscitation Module al-
lows the caregiver to administer forced breathing if required. The Resuscitation Module may feature
either a traditional bag and mask technology or a T-piece technology.
An additional feature, unique among warmers is the Hands Free Alarm Silence. This is a standard
feature on both warmers. Alarms may be silenced just as they would with the alarm silence button,
but without touching the unit. The proximity sensor for the Hands Free Alarm Silence is located in the
alarm light panel. The alarm can be silenced by gently waving ones hand approximately two to six
inches in front of the sensor. Both units also have a conventional alarm silence button as an alternate
way of silencing alarms.
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1.1.2 Mechanical Controls and Cable Connections
1 1
2
3
4
5
6
7
Feature Description
number
1 Two dimmable observation lights
2 Aimable procedure light
3 Procedure light On/Off switch
4 Color display screen
5 Resuscitation system (optional)
6 Bed, with integrated scale
7 Front bedside panel
8 Bed tilt control lever
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22
21
20
10 19
18
11
12
17
16
15
14
13
Fig. 2: Panda iRes Warmer, side view
Feature Description
number
9 Recessed radiant heater
10 Side bedside panel
11 Front handle
12 Pass through drawer
13 Two bed height adjustment pedals, up and down
14 Four caster wheels
15 Four brakes
16 Elevating column
17 Tank guard (optional)
18 Scale cable connector
19 Temperature probe Jack
20 High pressure air/oxygen yoke (optional)
21 Maneuvering handle and cord wrap
22 Dovetail rail
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Mechanical Controls and Cable Connections (continued)
Feature Description
number
23 RS-232 connector
24 Two accessory power outlets
25 SpO2 Jack
26 Removable rear bedside panel
27 Power cord inlet
28 Mains power switch
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1.1.3 Controls and Displays
6
7
8
3
10 11
1 9
Feature Description
number
1 Power stand-by switch - On the left below the display turns the power to the warmer
On and Off.
2 Oximetry key (optional) - This key retains the same function at all times.
3 Mode key - To select manual or baby mode. This key retains the same function at all
times
4 Temperature/power increase/decrease key - This key retains the same function at all
times
5 Baby temperature - Can be displayed in degrees Celsius or degrees Fahrenheit.
The default setting is degrees Celsius.
6 Alarm silence key - Alarms can be silenced by pushing the key above the display or by
a wave of your hand directly in front of the alarm light.
7 Help key - The key with the ? in the upper right corner brings up the help screen that
explains alarms and functions.
8 Task keys - The five keys on the right are soft keys that change their function de-
pending on what task you wish to perform. They control equipment settings and op-
tions.
9 Dimmer knob - On the right controls the brightness of the observation lights.
10-11 Date and time - Displayed at the bottom of the screen.
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Radiant heat from an infrared heat source is focused onto the bed to warm the patient. The operator may
select either the heater power (manual mode) or skin temperature (baby mode) control method. Depending
on the control method selected, the heater is either regulated at the operator selected power level or the
heater output is modulated to maintain the patients temperature at the value selected by the operator.
The Giraffe model is intended for use in a neonatal intensive care unit. It features a mattress which can be
rotated as needed by the operator to gain better access to the patient. Also included are general observa-
tion lights and a procedure light. The procedure light is mounted on a ball joint so that it can be directed
where needed on the bed surface.
The Panda iRes model is intended for use in a labor and delivery unit. It also includes the same general ob-
servation lights as the Giraffe Warmer, but the procedure light is optional.
Both units feature the same heater head to house the radiant heater. Due to the small size of the heater
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reflector and its compound elliptical shape, designed specifically for this product, the heater head is very
compact compared with other warmers currently on the market. This compact size limits the area the heater
head occupies over the bed surface. By leaving the area over the bed clear, the caregiver can observe and
treat the patient unobstructed. Additionally, this open area allows the head of an X-ray machine to be placed
over the patient without moving the heater head or patient.
Both units also feature optional integrated SpO2 and Resuscitation Modules. The SpO2 option allows the
caregiver to monitor the patients oxygen level, while the optional Resuscitation Module allows the caregiver
to administer forced breathing if required. The Resuscitation Module may feature either a traditional bag and
mask technology or a T-piece technology.
An additional feature, unique among warmers is the Hands Free Alarm Silence. This is a standard feature on
both warmers. Alarms may be silenced just as they would with the alarm silence button, but without touch-
ing the unit. The motion sensor for the Hands Free Alarm Silence is located in the alarm light panel. The
alarm can be silenced by gently waving ones hand approximately two to six inches in front of the sensor.
Both units also have a conventional alarm silence button as an alternate way of silencing alarms.
1.2.2 Rails
The rails support the heater head, resuscitation module, and probe panel assembly by connecting them to
the base assembly.
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available. One column type can be adjusted manually, and the other can be adjusted electrically by
foot pedal controls on the caster supports.
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1.3.2 Hands Free Alarm Silence
This processor-controlled circuitry resides on the Alarm Light Board (see Figure 7). The user input is ac-
complished with an infrared emitter/receiver pair. The emitter/receiver pair is monitored by the alarm light
microprocessor, which sends the alarm silence signal to the main application processor. The main applica-
tion processor uses this signal as one of two inputs to determine whether the alarm should be silenced. The
Hands Free Alarm Silence may be enabled/disabled/disengaged through Service Mode.
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1.3.3 Watchdog
The system incorporates smart monitoring mechanisms that allow three of the processors to monitor each other in or-
der to detect abnormal operation (see Figure 8). The audio processor functions as the master watchdog processor and
ensures the main application processor is responding normally. If the audio processor detects abnormal functioning of
the main processor it opens the heater safety relay and activates a high priority alarm.
The main application processor ensures the heat control processor is responding normally. If the main application pro-
cessor detects abnormal functioning of the heat control processor it opens the heater safety relay, activates the high
priority alarm and displays a system fail message. A power cycle is required to return the system to use.
An independent hardware circuit monitors the audio processor to ensure it is functioning normally. In the event the
audio processor does not respond normally the hardware circuit will reset the audio processor causing a system fail
condition. A power cycle is required to return the system to use.
NOTE: A system failure on the screen indicates the main application processor has detected abnormal
function in the system. A blank screen with a high-priority alarm indicates a problem with the
main application processor.
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Fig. 8: Watchdog
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A power fail is detected when the audio processor (see Figure 10) senses the 3.3 Volt power supply below normal oper-
ating level with the stand-by switch on. This will result in a shut down of the main application processor and initiate a
power fail alarm for a minimum of 10 minutes. The lithium ion battery or the super capacitor provides power for the
alarm. The audio signal for a power fail alarm is a repeating sequence of 3 beeps from a piezoelectric buzzer on the
Alarm Light Board. The visual signal is one LED on the Alarm Light Board.
The heat control processor on the Power Board has an independent circuit to detect a drop in 12 Volt power below
normal operating levels. In the event of low 12 Volt power the heat control processor will initiate a controlled shutdown
of the heater circuit. In the event of an internal malfunction resulting in loss of one level of DC power, one or more of the
processors will shut down causing the smart monitoring function to initiate a system failure.
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1.3.6 External Communication
Serial communication is provided though the ThermaLink port (see Figure 11). A null modem cable is required for con-
nection to a PC serial port. Ethernet communications are not used at this time.
A string of ASCII characters will be transmitted over the RS-232 port every 15 seconds +/- 5 seconds.
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1.3.8 Display
The color VGA display is driven and powered by the Control Board. The Control Board includes a dedicated graph-
ics controller with on-board memory. The LCD is backlit with two high voltage CCFL tubes. The backlight inverter is
located on the Control Board.
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1.3.10 Elevating Base
The elevating base assembly is powered by mains power (see Figure 13). There are fuses for the mains power on the
Power Board. The power must be enabled by the elevating base relay on the Power Board. This relay is under the con-
trol of the main application processor. Footswitches on both sides of the unit control the elevating base movement.
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During Warmup Mode Check Baby alarms are deactivated. If you do not press the Admit Baby key during the
first minutes after start up, the display will show Warming... and the radiant heater will automatically run at 100%
power. After 7 minutes, the display indicates Warmup Complete and the default heater power setting drops to
50%. The display continues to flash Admit Baby until you press the Admit Baby key and start normal operation.
The user set point is heater output level from 0% to 100% in 5% increments. The main application software passes
the set point to the heat control processor. System input to the heat control processor also includes heater calibration
data from the EEPROM chip in the heat engine assembly. The heat control processor modulates, in line cycles, the
power to the heater with a solid-state relay to achieve the desired power output. Power to the heater is monitored
with a solid-state power meter to ensure the proper power is being delivered.
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1.3.13.3 Baby Mode
The heat control processor functions identically in Baby and Manual Modes. The user input to the system in Baby
Mode is the desired skin temperature. The system measures actual skin temperature via the patient probe. The sig-
nal is an input to the Control Board converted to a digital signal read by the main application processor. The proces-
sor utilizes a proprietary, patented heat control algorithm to determine the optimum heater output power. This output
power is passed to the heat control processor.
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1.3.13.4 Start-up
When the unit powers on, there are a number of self-tests that occur; these are the Power On Self Tests (POST). If a
failure is detected during POST the unit will display a system failure message on the screen, record the event in the
error log and initiate a high priority alarm. If no failures are detected, normal startup operation as defined in the user
manual will commence.
The system incorporates a safety relay that interrupts power to the heater if one of the following conditions occurs:
1.3.14 Scale
The scale communicates with the main processor via RS-485 (see Figure 18). The connector for the scale cable is in the
probe panel housing. The scale is powered by 12V DC supplied by the control board. The power circuit includes over-current
protection.
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1.3.15 SpO2
The Pulse Oximetry (SpO2) option utilizes an OEM module commonly used in other monitoring equipment. For units that
have the SpO2 option, the SpO2 patient probe connects to the SpO2 module which is located in the probe panel housing
(see Figure 19). The probe panel housing contains the OEM module and an SpO2 interface board. Oximetry parameters
and alarms are passed to the main application processor via serial communication. The OEM module output is commu-
nicated to the user visually or audibly as required.
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1.3.16 Alarms
Alarms are indicated to the user both visually and audibly. Visual alarms are provided via the LED Array located on the
Alarm Light Board (see Figure 20). The LED array is controlled on and off by the alarm control signal provided by the
main application processor or audio processor on the Control Board. Alarm audio isgenerated by an audio amplifier
also under control of the audio processor in response to a command from the Main Application Processor.
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1.3.17 Equipment Grounding
Grounding and Insulation Design for Safety
The grounding and insulation design of the Giraffe and Panda Warmers ensures all mains circuitry is separated from
the operator and patient by one of two methods:
The radiant heater reflecting dish, heater duct, electrical enclosure, and elevating base all rely upon basic insulation
of the wires and a grounded metal barrier.
The heater head housing and main bracket (on elevating base models) rely on double/reinforced insulation. For the
heater head housing, the two parts of the housing along with the wire insulation form a double insulation system. For
the main bracket, a sheet of insulating material is fitted between the bracket and the elevating column. This insula-
tion, along with the insulation on the wires of the elevating base form a double insulation system.
The device incorporates grounding for ESD/EMC compliance. The dovetail rails and legs of the device are grounded to
comply to ESD susceptibility standards.
The device incorporates IEC appliance outlets for attachment of approved accessories that include a third wire
ground. The device also incorporates a ground equalization potential post, which allows for the interconnection of
equipment grounds if required.
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Section 2
Checkout and Installation
2.1 Warmer Maintenance Schedule
The unit should be maintained in accordance with the preventative maintenance procedures detailed in
this Service Manual. Service maintenance must be performed by a technically competent individual. The
Checkout must be performed after installing the warmer.
This schedule lists the minimum frequencies. Always follow hospital and local regulations for required fre-
quencies.
Inspect suction tubing that is routed through the dovetail rail. Replace the tubing as described in the clean-
ing instruction in the resuscitation operator supplement, as required.
This schedule lists the minimum frequencies. Always follow hospital and local regulations for required fre-
quencies.
2.1.4 Annually
Perform the electrical safety checks as described in this service manual (refer to sections 2.3.
Calibrate the scale as described in this service manual (refer to section 3.1).
Perform the resuscitation system service checkout as described in the Resuscitation Systems service manual.
Replace the lithium ion battery as described in this service manual (refer to section 5.2.3).
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NOTE: T he lithium ion battery is used to sound the power failure alarm and to power memory circuits
during a power failure
Perform the complete blender maintenance as described in the Resuscitation Systems service manual.
NOTE: The resuscitation systems service tools are described in the Resuscitation Systems service manual.
warning:
Do not perform the preoperational checkout procedure while the patient occupies the unit.
warning:
Complete the preoperational checkout procedure section of this manual before putting the unit into opera-
tion. If the equipment fails any portion of the checkout procedure it must be removed from use and repaired.
1- Disconnect the power cord for the mechanical portion of the preoperational checkout procedure.
2- Examine the power cord for any signs of damage. Replace the cord if damage is evident.
3- Check that the cord retainer/accessory outlet guard on the back of the control panel is in place.
4- Examine the unit overall for any damaged or missing parts.
5- C
heck that all the casters are in firm contact with the floor and that the unit is stable. Lock the caster
brakes and check that they hold the unit in place. Release the brakes and check that the unit moves
smoothly.
6- C
heck the operation of all four bedside panels. The bedside panels should lock securely in the upright
position.
7- C
heck the operation of the bed tilt mechanism. When you squeeze the tilt control and push down on
the foot of the bed the head of the bed should raise easily, and should stay in position at any angle
along its tilt path when you let go of the tilt control. The bubble levels on the side bedside panels indi-
cate the mattress is level.
8- C
heck the movement of the Procedure Light Assembly (if equipped). Ensure movement is smooth and
the light can be positioned at each corner of the mattress.
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2.2.2 Controller checks
warning:
Do not use the warmer in the presence of flammable anesthetics; an explosion hazard exists
under these conditions.
warning:
Always connect the warmer directly to a hospital grade wall outlet . Connecting to a power strip
or another piece of equipment may result in safety and ground integrity issues.
1- M ake sure the power cord is connected to the outlet on the unit and to the rated power supply.
2- S witch on the power at the mains switch on the back of the unit, and at the standby switch on the
front control panel. Verify the following:
All the displays and indicators light
The software revision appears
The prompt tone begins
3- P ress the Admit Baby key to enter normal operation in Manual Mode. Select Heater Power percent-
age to silence the prompt tone.
4- C onnect the baby temperature probe to the jack on the right side of the bed. If using a warmer with an
In-bed scale, the temperature probe jack is located above the In-bed scale connection.
5- C heck the patient probe. Warm it by placing it between your fingers, and verify that the baby tem-
perature reading increases.
6- U nplug the patient probe and change the warmer to Baby Mode. Check that both visual and audio
alarms trigger in the Baby Mode. Silence the alarm by using either the alarm silence key or the Hands
Free Alarm silence.
7- R eturn the warmer to Manual Mode by pressing the Mode key. Select a Heater Power setting to
silence the prompt tone.
8- If the unit is equipped with an elevating bed, check the operation of the bed elevation mechanism.
Raise and lower the bed along its entire travel range, checking that the mechanism operates smooth-
ly. Check that the raise and lower bed pedals on both sides of the unit raise and lower the bed height.
9- If either the scale or oximetry option is installed, push the About key on the main help menu and
check to ensure that their current software revision appears.
10- Check the Observation Lights function and Procedure light function (if equipped).
NOTE: Not all metal components are safety ground bonded. Only the heater reflector, heater
duct, power supply mounting bracket(s), electrical enclosure and elevating base are re-
quired to be safety ground bonded. When servicing involves disturbing the ground bonds
of these components the ground integrity should be verified.
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2.3.2 Earth Leakage and Chassis Leakage current
Patient lead leakage current shall be measured between all the leads of the SpO2 connector shorted to-
gether (service tool part number 2006036-001) and ground.
NOTE: The isolation of the patient temperature probe is dependent upon the insulation of the
patient temperature probe. These probes are 100% tested and do not require retesting. If
so desired, the patient temperature probe can be tested by wrapping in foil or submerg-
ing in normal saline 6 inches (15 cm) of the part of the probe that attaches to the patient.
Measurements shall be taken from the conducting medium. The patient lead leakage cur-
rent limits listed above are applicable.
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Section 3
Calibration
3.1 Scale Calibration
NOTE: The scale is calibrated using a Class F calibration weight between 1 kilogram and 8
kilograms (accuracy of 0.01%).
1- Hold the help key (?) and the alarm silence key while powering up to enter the service mode.
2- On the main menu, select Calibration, then select Scale Manual cal.
3- Use the up and down arrows to select the gram value of the known test weight.
4- When prompted, clear all objects from the bed. Select start. Scale will obtain tare.
5.- Place the test weight on the center of the bed.
6- Press select and calibration will begin. Display will indicate when successful calibration is completed.
7- Turn off the power to exit the service mode.
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Section 4
Troubleshooting
4.1 Service Mode
To access the main service mode turn on the unit and hold the (?) and Alarm Silence (A) keys for approxi-
mately 10 seconds after you see the Giraffe/Panda logo screen. From the main menu select keys for user
settings, unit specific information, calibration, time settings and diagnostics . See figure 4.1. To exit the ser-
vice mode, power down the unit.
NOTE: Note: If the unit will not boot up, the service mode can be accessed by setting control board
dipswitch position one (1) to ON and turning on mains power. The default position of all 8
dipswitch positions is OFF.
To access the unit specific information, push the Help (?) key while in the service mode.
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Unit information displays:
Unit type
Software
Processor and option versions
PC Board IDs
Battery voltage status
Power fail minutes
Language
Settings Default
Patient temp alarm 0.5C / 1.0C 1.0C
CPAD (check patient alarm disabled) 5% - 50% 25%
Man temp alarm Off / 0.5C / 1.0C Off
Touchless silence Enable / Disable Enable
Bed elevate Enable / Disable Enable
Temp units C/F C
Scale Units grams / lbs-oz grams
Scale Resolution 10/5 grams 10 grams
Time Format 12/24 24
Low pulse limit 0 - 110 100
High pulse limit 111 - 240 200
Low sat limit 0 - 99 85
High sat limit 86 - 105 100
SpO2 averaging 2-4 / 8 / 16 8
SpO2 sensitivity Normal / Maximum Normal
Pulse tone volume, Panda iRes unit 0/ 1 / 2 / 3 / 4 1
Pulse tone volume, Giraffe unit 0/ 1 / 2 / 3 / 4 0
Alarm volume 0/1 / 2 / 3 3
Language Many English
4.1.3 Calibration
Allows the user to calibrate the Scale either using a known weight which is configurable or by resetting it to
factory calibration.
4.1.4 Date/Time
Allows the user to set the unit displayed Month, Year, Day, Hour, and Minute.
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4.1.5 Diagnostics
The Diagnostic Utilities are used to determine the overall health of the system from an electronic and soft-
ware stand point. Available Utilities are as follows:
A. A DC Channels The ADC Utility provides the means to display A to D values for the patient probe thermistors, fixed
reference A to D input, Control Board Temperature (Ambient Temperature) as well as A to D reference voltage.
B. VGA Test The VGA Test Utility instructs the display processor to display a color test pattern of all black, red, green,
blue and gray. Once invoked, each pattern is stepped through by pressing the up/down keys on the Touch Panel.
C. Touch Panel The Touch Panel Utility is an interactive utility which displays the real time status of the touch panel
buttons.
D. Scale A/D Values The Scale A/D Values Utility displays the raw counts and corrected values based on calibration
and used by the software to calculate the displayed value.
E. Audio Test The Audio Test Utility allows the user to invoke the Low Priority Alarm, High Priority Alarm and Pulse
Tone.
F. Odometer The Odometer Utility displays minutes of operation in both a re-settable and non-re-settable format as
well as minutes of operation at 10 to 100% power output in 10% increments.
G. Logs The Logs Utility displays System Fail Messages which are stored in a first in, first out format and is limited in
size.
H. Heat Engine Check When the Heat Engine Health Check Diagnostic is started the main processor sends a com-
mand to the Heat Control Processor to Set the output to 25%. The measured output is then monitored and dis-
played. Stop sets the output to 0%. The acceptable output is between 24 and 26 percent. Commands: Start; Stop;
Exit.
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4.1.6 Diagnostics using serial port
Using a PC and null modem cable gives access to an additional diagnostic screen that allows you to update
system software, access logs and perform other commands not available on the units service mode screen.
1. Connect the cable to the 9 pin serial port located on the back of the warmer to a windows
based PC.
2. Open Hyper Terminal (Start/All Programs/Accessories/Communication/)
3. Provide a name in the resulting dialog and click ok.
4. In Connect Using Select COM 1
5. Enter Bits per second 115200
Data bits 8
Parity None
Stop bits 1
Flow control None
Click OK
6. Boot Warmer into Service Mode SW if not already.
7. Press enter on your computer.
8. Type help and press enter to see available commands Note: The LOGS command will display 6 log
types using the following parameters: POW_UP, BUT_PUSH, ALARM, SILENCE, SYSFAIL, STATE, CF
Note: Typing LOGS will capture all data. Data transfer may take up to 15 minutes.
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Data received via the LOGS command will contain multiple entries formatted in the following fashion:
The first four sections (Date, Time, Temperature, Log Type) are consistent for every entry and have the following values
Auxiliary data consists of 10 data bytes represented in hexadecimal format. These data bytes have different meanings
depending on the Log Type, as defined below. If the data byte is not listed, its value is a dont care.
Byte 1 The stage of the alarm. A 1 indicates the alarm has just occurred.
A 2 indicates the alarm has progressed because the alarm condition
has not been alleviated or the alarm has not been silenced.
Byte 1 The stage of the alarm. A 1 indicates the alarm has just occurred. A 2 indicates
the alarm has progressed because the alarm condition has not been alleviated or the alarm
has not been silenced.
SYSFAIL Bytes 0-3 The auxiliary data associated with the system failure.
Byte 4 The system failure number which corresponds to the values found Table 4.3.
STATE Bytes 0-3 The patient set point listed in hexadecimal byte-swapped format.
Note: No decimal place is present (6d 01 00 00 can be looked at as 0x0000016d
which translates to 365 or 36.5 degrees C)
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Control Board
TP Value
1 +3.3V (analog)
2 Ground (analog)
3 +2.5V (digital)
4 Ground (digital)
5 +1.8V (digital)
TP 1, 2
6 + 5V (isolated)
10 Ground (isolated)
TP 3, 4, 5
7 +12V (digital)
8 Ground (digital)
9 +3.3V (digital)
11 Ground (digital)
12 +5V (digital)
13 +3.3V (standby)
TP 7, 8, 9 TP 6, 10 TP 11, 12 TP 13
Power Board TP 26 TP 25
Pin 1
TP Value
20-1 Ground (DC)
20-2 +5V
20-3 +12V
22-1 Ground (DC)
22-2 +3.3V
22-3 +12V
25-1 Ground AC
side (not
TP 20 connected to
earth)
TP 22
25-7 5V - ni
TP 21
Pin 1
TP 29
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Confirm Probe Jack Connec- Not getting a reading Bad probe Replace patient probe
tion from either thermistor in
temperature probe
Bad harness Check patient probe cable going
to J54 on probe panel interface
board.
Bed does not tilt Disconnected control Check that cable terminators are fully
cable seated in retainers
Hands free alarm silence does not Function has been dis- In setup verify touchless silence is en-
work abled abled.
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Neither of the observation lights will Bad harness connection Be sure that connectors at J24, J25, J26
light. power pc board are seated properly.
One of the two observation lights will Bad bulb Remove bad bulb and install new bulb.
not light
Bad socket Disconnect 2 pin connector at bulb
socket. With good bulb installed check
continuity through bulb.
Procedure light will not light. Bad bulb Remove bad bulb and install new bulb.
Bad fuse on power board Check for mains voltage at power supply
so no mains power to input connector pins 1-3. If not present
procedure light power check fuses F3, F6.
supply.
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Elevating column does not go up or Bed elevate is disabled In setup screen verify that elevate is
down with any of the four footswitch- in service or operator enabled
es. screens
Elevating column does not go up or Is there mains voltage to Measure voltage at IEC connector on
down with any of the 4 footswitches. the column? eBase supply cord. If AC voltage is not
present, skip to No power to column.
Elevating column does not go up or Defective column. Disconnect harness from 3 pin connector
down with any of the 4 footswitches. going into column. Short pins 2-3 On the
Mains voltage is input to column. column connector. Column should raise.
Short pins 1-3 and column should lower.
If not column is defective.
Elevating column does not go up or Defective footswitch Test the switch and the harness with an
down with any of the 4 footswitches. harness ohmmeter.
Mains voltage is input to column.
One of the 4 footswitches does not Defective footswitch or Test the switch and the harness with an
raise or lower the elevating column. harness. ohmmeter.
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Section 5
Repair Procedures
SENSITIVE TO ELECTROSTATIC DISCHARGE CAUTION:
Use the static control work station (Stock No. 0175-2311-000) to ensure that static charges are safely
conducted to ground and not through static sensitive devices The velostat material is conductive; do not
place electrically powered boards on it. Whenever this Electrostatic Discharge (ESD) symbol appears beside a
procedure, take static control precautions.
NOTE: P rior to returning a unit to service after performing any repair or calibration, always perform the
service checkout procedure and electrical safety check.
NOTE: Take care to not cross thread or over tighten the captive screws.
NOTE: F or easier access to the heater housing during repairs, you may wish to lower the warmer bed to its
lowest position.
1- U
se a 3mm hex key to remove the 8 socket head screws, split ring washers and flat washers that secure
the upper heater housing to the lower housing and remove the upper heater housing. Lift the upper
housing from its top, front edge (removing the top of the housing allows access to the heat engine,
heater protective grill, power supplies, and alarm light board).
warning:
The heat engine, exhaust duct and protective grill may still be hot if you disassemble the unit immediately
after it has been in use.
1.- Two of the screws that secure the duct are behind the power supply mounting plates. To access the
two screws behind the power supply mounting plates, remove the two mounting plate screws and
place the power supplies to the side. Remove heat engine wires from clip. Disconnect the thermostats
on either side of the exhaust duct and the ground wire attached near the bottom left of the duct. Use a
3mm hex key to remove the 6 socket head screws, split ring washers and flat washers that secure the
exhaust duct to the lower heater housing and remove the duct. If the unit has been used recently the
duct may be hot.
2- If removing the heat engine disconnect the heater power connectors and ground wire. Remove the 3 hairpin cotter
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pins located under each of the heater adjustment screws and remove the assembly . You may need to cut safety
wires that secure the adjustment screws. These are for shipping purposes and need not be replaced.
3- T o remove the heater protective grill, use a small straight screwdriver to lever open the 8 clips that hold it in place.
First push the grill wires down from the top of the unit, then pull them back up with pliers to make the clips easier to
grab with the pliers. When reassembling be sure the two grill wires that poke through the lower housing on either
side of the duct are on the outside of the ducts edges.
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Fig. 5-1: Heater housing, rear view NOTE: Upper housing, heat engine and
exhaust duct are not shown, for visibility
NOTE: If the laser dot is within the target area no further action is required
NOTE: Standard laser tool batteries require replacement after approximately 20 minutes of use.
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5- U
se a long 3 mm hex key to adjust the dishs 3 adjustment screws located in the bosses underneath
the cotter pins. Loosening or tightening the 2 screws on either side will move the laser spot from left to
right, with longitudinal shift, and adjusting the screw in back moves the spot up and down in the tar-
get. Adjust the side screws first, then adjust the bottom screw, so that the spot is near the center of the
target.
NOTE: If the laser dot is within the target area no further action is required.
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5.1.5 Alarm light board replacement (Figures 5-3 and 5-5)
1- Remove the upper heater housing. See section 5.1.1
2- R emove the 2 captive screws that secure the electronic enclosure on either side of the lens. Tilt the
top of the Electronics Enclosure out to allow access to the screws securing the back of the Alarm Light
Board.
3- T o remove the Alarm Light Board, use a 2mm hex key to remove the two screws that secure the Alarm
Light Board to the Electronic Enclosure. Disconnect its electrical connectors. When replacing the Alarm
Light Board, reconnect the ribbon cable first. When installed the LEDs will be oriented on the bottom of
the board.
1- U
se a straight blade screwdriver to remove the knurled screw that secures the light tunnel to the lower
heater housing, tilt the tunnel forward and take it out of the housing.
2- Disconnect the bulb electrical connector and slide the bulb from its spring retainer.
3- After replacing the bulb, confirm that the glass lens is properly aligned.
1- U
se a 3mm hex key to remove the single socket head screw that holds the procedure light in place. This
will allow the entire lamp to dangle by its connecting wires.
2- Push on the lever arm of the spring clip to eject the bulb from its holder.
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NOTE: Before installing the bulb it is necessary to move the lever back to its original position.
5.2.3 Lithium ion battery replacement (Figures 5-3, 5-4 and 6-14
1- L oosen the 2 captive screws at the top of the enclosures rear panel, then tilt the panel down and lift the
2 tabs at the bottom of the panel up out of the slots that they seat in.
2- Loosen the 4 captive screws that secure the power board panel and tilt it down away from the unit.
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3.- Note the polarity and be sure to install the new lithium ion battery with the same polarity. When replac-
ing the battery use a small screwdriver to slide the old lithium ion battery out of its holder.
Caution:
The replacement lithium ion battery must have heat shrink around the battery to avoid possible battery
damage if it is incorrectly installed.
CAUTION:
Dispose of the battery in accordance with local toxic waste regulations.
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13- U se a 5.5 mm socket to remove the KEPS nut from the inside of the enclosure that secures the touch
panel. Disconnect the touch panels electrical connectors and remove touch panel.
14- If replacing the LCD display, use a 2 mm hex key to remove the 4 button head screws, split washers and
flat washers that secure the display. Disconnect its 3 electrical connectors and remove the display.
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3- Use a 5.5mm wrench to remove the 2 KEPS nuts the secure the outlet panel.
4- Loosen the 4 captive screws that secure the power board panel.
5- Lift the outlet panel off the studs and flip it down.
6- T o remove the speaker, disconnect its electrical connector, then use a 2mm hex key to remove the 2 but-
ton head screws, split ring washers and flat washers that secure it to the panel.
7- Use a 10 mm wrench to remove the ground stud nut and star washer.
8-The circuit breakers, power inlet and line filter can be disconnected and popped out of their cutouts in
the panel.
9- T o release the accessory outlets push in the pins that secure them in their panel cut outs. Accessory out-
let circuit breakers are not snap in, they require removal of a dress nut.
10- T o remove the RS-232 connector, slide the two moveable pins right so that the rigid pins can clear the
edge of the cutout, and press down on the 2 remaining pins.
1- Remove
the rear bedside panel by pushing the release button behind the bed, and lifting up the bedside
panel.
2- For better access, tilt the bed so the back is down and the front is all the way up.
3- U
se a 3mm hex key to remove the 4 socket head screws, split ring washers, and flat washers that secure
the bottom half of the probe panel housing.
4- Remove the bottom half of the housing by sliding it forward towards the bed.
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1- R emove the bottom end cap from the West Dovetail Rail and remove the decorative strip so that the
SpO2 ground wire screw can be accessed.
2- Remove the SpO2 ground wire screw.
3- Disassemble the probe panel housing following instructions 5.3.1.
4- R emove the two button head screws securing the metal housing to the top of the Probe Panel housing
using a 2mm hex key. Note location of ground strap for re-assembly.
5- Unlatch and disconnect the SpO2 cable leading to the east dovetail rail.
6- Disconnect the SpO2 Flex Circuit connector.
7- R emove the metal housing/Sp02 assembly and separate the two halves of the metal housing.
8- T o replace the board assembly use a 2 mm hex key to remove the 4 socket head screws and the lock
tooth washers that secure the SpO2 interface board to the metal housing.
9- Reverse the above procedure to reinstall SpO2 board.
1- R
emove the bottom end cap from the West Dovetail Rail and remove the decorative strip so that the
SpO2 ground wire screw can be accessed.
2- Remove the SpO2 ground wire screw.
3- Disassemble the probe panel housing following instructions 5.3.1.
4- Unplug the Flex Circuit from the SpO2 Board.
5- R emove the Flex Circuit/Plate Assembly from the Upper Housing by pulling on the plate. This a friction fit
that my require some force.
6-Remove the Blue Connector end of the Flex Circuit by carefully prying the connector off the plate.
Save the plate for re-assembly.
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1- U
se a 4 mm hex key to remove the 3 socket head screws, split ring washers and flat washers that hold
the storage module to the main bracket (see Figure 5-8). The storage module rests on the bracket and
will stay in place until you slide it forward. Check that the drawers are empty of heavy objects.
2- S
tanding in front of the unit, grasp the storage module on both sides and remove it by sliding it forward.
3- U
se a 13 mm wrench to remove the nut and split ring washer that secures the gas tilt cylinder from the
main bracket.
4- Use a 4 mm hex key to remove the secondary bed locking mechanism from the main bracket.
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Mounting screw
locations Shroud
grasp
here
Drawers
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5- To remove secondary lock, squeeze the tilt release and slide the lock of its threaded strut.
6- U
se a 4 mm hex key to remove one screw, and loosen the other screw, that fasten each of the pivot
plates to the bottom of the bed on either side of the main bracket. Swing the plates aside so that the
bed can be lifted up off the pivot rod later.
7- The bed can be lifted off and turned over to access all the tilt parts.
1- If possible, lower the elevating column to the lowest position and disconnect the base power cord from
the back of the column. Lock all the casters.
2- U
se a 4 mm hex key to remove the 3 socket head screws, split ring washers and flat washers that hold
the storage module to the main bracket (see Figure 5-8). The storage module rests on the bracket and
will stay in place until you slide it forward.
3- S
tanding in front of the unit, grasp the storage module on both sides and remove it by sliding it forward.
4- U
sing a 6mm hex key, remove the 4 bolts that secure the top of the elevating column to the main
bracket. Tilting the bed forward allows easier access to the 4 screws.
5- W
ith the assistance of another person lift the upper portion of the warmer and move it to the side off the
base.
6- P
ry open the screw covers and loosen the 2 screws that secure the base shroud. Remove the base
shroud. Disconnect the footswitch connectors.
7- U
se a 6mm hex key to remove the 4 bolts that secure the column to the legs and remove the elevating
column. When reassembling, be careful not to cross thread 4 bolts that hold the elevating column to the
main bracket.
Increasing the bed height is relatively easy, since the spring force pushes the bed up. However, decreasing
bed height will require two people, unless a tool such as a ratchet strap is used to compress the spring and
lower the bed to the desired height.
Adjustment
1- The adjustment pin is held in place by retaining screws (with large diameter flat heads counter bored in the col-
umn) that fit into threaded holes in both ends of the pin. Use a large screwdriver to remove one of these slot head
retaining screws that are located on either side of the warmer, about half way up the column. It does not matter
which side of the column: either retaining screw can be removed. If the unit is equipped with a suction canister
bracket, you may wish to remove it.
2- Using a rubber hammer or mallet and a large screwdriver or punch, drive the pin out from the end with the retain-
ing screw removed (you may wish to hold the bed down so that it does not jam the screwdriver as the spring is
released).
3- Allow the bed to rise to the desired height. If possible, do not allow the bed to reach its highest point, where the
internal spring is fully extended, since this makes compressing the spring to lower the bed more difficult.
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NOTE: T
he best way to compress the spring is to push down on the main bracket casting directly
above the column. However, this spot is not easily accessible. A strong board or piece of
wood about a meter long can be passed under the bed across the top of the casting, then
both installers can press down evenly on both ends of the board, until the column reaches
the desired bed height.
4- While one installer holds the bed in position, the other checks the alignment of the holes on one side of the column,
and then drives in the pin. It may be necessary to use a small screwdriver or hex key as a lever to push up or down
on the pin end inside the column to align the pin and the holes on opposite side.
5- Re-install the retaining screw to secure the pin and lock the bed in place.
Section 6
Illustrated Parts
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6-2 Panda iRes & Giraffe Warmers M1128927 Rev. 02 2007 General Electric Company, all rights reserved.
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1- Screw, M3 x 8, Btn Hd.................. 6600-0706-405 16- Push-on clip, grill retainer ................M1079756
2- Washer, M3 X 3.2 ID, 0.5 ............ 6600-0712-402 17- Protective grill
3- Split ring washer, M3.................... 6600-0713-402 (order 12 pcs. item 16).............. 6600-2032-500
4- Thermostat..................................................M1074875 18- Observation light,
5- Screw, M4 X 12, Skt Hd................ 6600-0707-410 bulb replacement ................................M1121134
6- Split ring washer, 19- Observation light kit, right............ M1108233-S
M4 X 4.1ID, 0.9 ............................... 6600-0713-403 20- Observation light kit, left............... M1108234-S
7- Heater duct ..................................... 6600-2037-500 21- Procedure light kit..................................M1092567
8- Screw, M4 X 10 Btn Hd ............... 6600-0706-409 Procedure light
9- Lock washer, M4 Int Tooth......... 6600-0713-432 bulb replacement .................................M1121135
10- Heat engine kit 115V....................... M1110787-S Parts not shown
Heat engine kit 230V....................... M1110788-S Procedure light filler plate and mounting
11- Dish retaining pin........................ 6600-2096-500 hardware for units without option
12- Observation Light Brkt.............. 6600-2142-500 Plate................................................... 6600-2044-500
13- Screw, alignment......................... 6600-2101-500 Screw, M4 x 20 Btn Hd.............. 6600-0706-412
14- Cable clip....................................................M1085398 Split ring lock washer, M4........ 6600-0713-403
15- Nut, M4 X 0.7................................. 6600-0711-407 Washer, M4.................................... 6600-0712-403
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6-4 Panda iRes & Giraffe Warmers M1128927 Rev. 02 2007 General Electric Company, all rights reserved.
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*Includes 10 pcs 3.15 A, 10 pcs 2A, 5 pcs. 6.3A and 5 pcs. NANO2 2A
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2 3 4
20
19
18
17 21
16
15
3
2
14
13 22
12 23
24
30 25
28
Fig: 6-4b: Power board & outlet panel
27
29 26 Figure 6-4b: Power board & outlet panel
(Continued from previous page)
6-6 Panda iRes & Giraffe Warmers M1128927 Rev. 02 2007 General Electric Company, all rights reserved.
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6.3 Probe panel housing
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6.5 Bed Assembly
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1- Mattress, Giraffe...................................................................................6600-0689-800
Mattress, Panda ..................................................................................6600-2057-500
2- Mattress support plate, Giraffe.....................................................6600-1365-500
Mattress support plate, Panda......................................................6600-2058-500
3- Translation deck (Giraffe only).......................................................6600-1352-500
Mattress tray support........................................................................6600-1353-500
X-ray tray.................................................................................................6600-1334-500
Locking latch.........................................................................................6600-1363-500
Latch cover.............................................................................................6600-1364-500
Latch spring...........................................................................................6600-1079-400
4- Rear bed side panel assy., Giraffe................................................6600-2146-500
Rear bed side panel assy, Panda.................................................6600-2145-500
Rear bed side panel assy, tube management, Giraffe......6600-1655-500
Rear bed side panel assy, tube management, Panda.......6600-2063-500
5- Left/right bed side panel assy , Giraffe................................................ M1092331
Left/right bed side panel assy, Panda................................................. M1092338
Left/right HFOV sidepanel assy, Giraffe.............................................. M1092332
Left/right HFOV side panel assy, Panda............................................. M1092340
6- Front bed side panel assy, Giraffe......................................................... M1092335
Front bed side panel assy, Panda.......................................................... M1092342
Front bed side panel assy, tube management, Giraffe...............M1092337
Front bed side panel assy, tube management, Panda................M1092506
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6.8 Accessories
Ancillary Equipment
6.9 Labels
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F6
F5
F4
F10
F9
F7 F8 F11 F12
FUSE SUBMINI 3.15A HIGH BRK...................................................................................................... F2, F3, F5, F6
FUSE, 2A, 125V, SMD, fast acting, socketed.............................................................................................F7, F8
6.3A 250V TIME LAG......................................................................................................................................... F9, F10
FUSE, Submini 2A..............................................................................................................................F1, F4, F11, F12
6-18 Panda iRes & Giraffe Warmers M1128927 Rev. 02 2007 General Electric Company, all rights reserved.
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6.11 Wiring Diagram WAIN229
(Print on 11x17 paper)
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Appendix A
Specifications
Power Requirements and Accessory Outlets
Power Requirements Accessory Outlets
5.25 A @ 100v ~, 50/60 Hz 2 A @ 100v ~, 50/60 Hz
4.57 A @ 115v ~, 50/60 Hz 2 A @ 115v ~, 50/60 Hz
2.39 A @ 220v ~, 50/60 Hz 1A @ 220v ~, 50/60 Hz
2.28 A @ 230v ~, 50/60 Hz 1 A @ 230v ~, 50/60 Hz
2.19 A @ 240v ~, 50/60 Hz 1A @ 240v ~, 50/60 Hz
Standards
Designed to meet requirements of:
IEC 60601-2-21 with amendment UL 60601-1
IEC 60601-1 with amendment BSEN - 45501 with amendment
IEC 60601-1-2 with amendment
Operating Environment
Temperature 18 to 30C
Humidity 5 to 75% Non-condensing relative humidity
Pressure 70-106 kPa
Air Velocity up to 0.3 m/sec.
Storage conditions
Temperature -25 to 38C
Humidity 0 to 85% Non-condensing relative humidity
Pressure 50 to 106 kPa
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Performance
System
Heater Element 360 Watts
Heater Output 27 mW/cm2
Patient temperature measure- 0.3C @ 30C to 42C
ment accuracy
Temperature probe accuracy 0.1C @ 30C to 42C
Observation Light 2 dimmable 35W halogen bulbs; estimated life 3000 hrs based on manufacturers
specifications
Procedure Light 2000 lux* average; estimated life 3000 hrs.
Mechanical Specifications
Height: 193 - 218 cm
Width: 64 cm.
Depth: 119 cm
Weight: 100 kg
Panda iRes Mattress Size: 66 x 48 x 2 cm
Giraffe Mattress Size: 65 x 48 x 4 cm
Bed Capacity: 14 kg
Bed Tilt: +/- 12 degrees continuous tilt
Accessories
Storage drawer package 6.8 kg maximum load
Combined accessory rails: 22 kg maximum load; no more than 19 kg maximum load on either rail.
A-2 Panda iRes & Giraffe Warmers M1128927 Rev. 02 2007 General Electric Company, all rights reserved.
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Appendix B
Electromagnetic Compatibility
warning:
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed
and put into service according to the EMC information provided below.
warning:
Portable and mobile RF communication equipment can affect Medical Electrical Equipment.
Caution should be use when operating such devices around Medical Electrical Equipment
warning:
This equipment/system is intended for use by healthcare professionals only. This equipment sys-
tem may cause radio interference or may disrupt the operation of nearby equipment. It may be
necessary to take mitigation measures, such as re-orienting or relocating the equipment/system or
shielding the location.
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Electromagnetic Emissions
RF emissions CISPR Group 1 The Giraffe Warmer uses RF energy only for its internal function.
11 Therefore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
RF emissions CISPR Class A The Giraffe Warmer is suitable for use in all establishments, other
11 than domestic and those directly connected to the public low volt-
age power supply network that supplies buildings used for domestic
purposes.
Harmonic emissions Class A
IEC 61000-3-2
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Electromagnetic immunity
Electrostatic dis- +/- 6kV contact +/- +/- 6kV contact Floors should be wood, concrete or ceramic
charge (ESD) IEC 8kV air +/- 8kV air tile. If floors are covered with synthetic
61000-4-2 material the relative humidity should be at
least 30%.
Electrical fast +/- 2kV for power +/- 2kV for power supply Mains power quality should be that of a typi-
transient/burst IEC supply line. line. cal commercial or hospital environment.
61000-4-4 +/- 1kV for input/ +/- 1kV for input/output
output line. line.
Surge +/- 1kV differential +/- 1kV differential Mains power quality should be that of a typi-
IEC 61000-4-5 Mode. Mode. cal commercial or hospital environment.
+/- 2kV common +/- 2kV common mode
mode line. line.
Voltage dips, short <5 % Ut(>95 % dip <5 % Ut(>95 % dip in Ut) Mains power quality should be that of a
interruptions and in Ut) for 0.5 cycle for 0.5 cycle typical commercial or hospital environment.
voltage variations 40 %Ut (60 % dip in 40 %Ut(60 % dip in Ut) If the user of the Giraffe warmer requires
on power sup- Ut) for 5 cycles 70 for 5 cycles continued operation during power mains
ply input lines IEC % Ut(30 % dip in Ut) 70 % Ut (30 % dip in Ut) interruptions, it is recommended that the
61000-4-11 for 25 cycles <5% for 25 cycles Giraffe warmer be powered from an uninter-
Ut(>95% dip in Ut) <5% Ut (>95% dip in Ut) ruptible power supply or a battery.
for 5 sec. for 5 sec.
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Electromagnetic immunity
3 Vrms
Conducted RF
150 KHz to 80 3V Recommended separation distance
IEC 61000-4-6
MHz
d = 1.2 P
3 V/m
Radiated RF
80 MHz to 2.5 3 V/m
IEC 61000-4-3
GHz
Radiated RF can affect the accuracy of
3 V/m 3 V/m in-bed-scale readings. However, the in-bed-scale is not
IEC 60601-2-21
26 MHz to 1 GHz normal operation critical to the performance of the Giraffe warmer unit
10 V/m 10 V/m (see Note 1 on page B-5).
26 MHz to 1 GHz no hazard
d = 1.2 P = 26 MHz to 800 MHz
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NOTE 1: Portable and mobile equipment can affect medical electronic equipment.
NOTE 2: A
t 80 MHz and 800 MHz, the higher frequency range applies. These guidelines may not
apply in all situations. .
NOTE 3: E
lectromagnetic propagation is affected by absorption and reflection from structures,
objects, and people.
NOTE a: F ield strengths from fixed transmitters such as base stations for radio, cellular/cordless
telephones and land mobile radios, amateur radios, AM and FM radio broadcasts and TV
broadcasts cannot be predicted theoretically with accuracy. To assess the electromag-
netic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the Giraffe warmer unit
is used exceeds the applicable RF compliance level above, the unit should be observed to
verify normal operation. If abnormal performance is observed, additional measures may
be necessary, such as re-orienting or relocating the Giraffe warmer.
NOTE b: Over the frequency range 150 KHz to 80 MHz field strengths should be less than 3 V/m.
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For transmitters rated at a maximum output power not listed above, the recommended separation
distance (d) in meters (m) can be determined 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.
NOTE: At 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
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Appendix C
Conforming with Standards and Directives
GE Healthcare has declared that this product conforms with the European Council
Directive 93/42 EEC Medical Device Directive when it is used in accordance with the
instructions provided in the Operation and Maintenance Manual..
This symbol indicates that the waste of electrical and electronic equipment must not
be disposed as an unsorted municipal waste and must be collected separately. Please
contact an authorized representative of the manufacturer for information concerning
the decommissioning of your equipment.
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Appendix D
Alarm Priorities
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Priority Alarm Subject Activation Criteria Message Displayed Silence Sound: Notes/Comments Indication Special Require-
Time 1= High, Light ments
2=Low, 3=
informa-
tional
1 SpO2 lost com- SpO2 board has Oximetry System See 1 When this alarm occurs, the Primary
munications not communicated Failure notes SpO2 module will be take out of
with the main pro- service and SpO2 options will
cessor for at least no longer be available. When
2 seconds silenced, the alarm will clear.
M1128927
Rev. 02
3 Oxygen satura- SpO2 <85 (floats Low SpO2 3 min 1 Primary
tion with user adjust-
able limits)
4 Check baby Radiant % power Check Baby - Heat 15 min 1 Primary Operational in
@ 100% for >15 Off Baby Control
min and alarm not mode
silenced
5 Check baby Radiant heater Check Baby - Heat 15 min 1 Primary Operational in
% above Check Off Baby Control
Baby Alarm Dis- Mode
abled (CPAD) limit
for >15 min and
alarm not silenced
6 Baby tempera- >2.0 from Control Baby Hot-Check 5 min 1 With hysteresis to avoid nui- Primary Operational in
ture Temp Temp Probe sance alarm recurrence after Baby Control
silencing. Hysteresis set at 0.2C Mode
- alarm clears at 1.8C
M1128927
8 Check baby Radiant % power Check Baby 12 min 2 Primary Operational in
@ 100% for > 12 Baby Control
min Mode
Rev. 02
% above Check Baby Control
Baby Alarm Dis- Mode
abled (CPAD) limit
for > 12 min
10 Temperature Two Thermistors in Temp. Probe Failure 2 min 2 to 1 Primary Operational in
probe failure a probed differ by (after 30 Baby Control
0.5 C or more. secs. mode or Manual
Mode when
Manual Temper-
ature alarm set
M1128927
13 Baby tempera- < 1.0C (<0.5C) Baby Cold - Check 12 min 2 With hysteresis to avoid nui- Primary Operational in
ture from control temp Temp Probe sance alarm recurrence after Baby Control
silencing. Hysteresis set at 0.2C Mode
- alarm clears at 0.8C (0.3C)
Rev. 02
14 No SpO2 probe Masimo board No SpO2 Board 3 min 2 to 1 Primary Only available if
connected indicates no board (after 10 SpO2 is running
connected secs)
15 Defective SpO2 Masimo board Check SpO2 3 min 2 to 1 Primary Only available if
probe indicates defective (after 10 SpO2 is running
probe secs.)
16 SpO2 interfer- Masimo board Check SpO2 3 min 2 to 1 Primary Only available if
ence detected indicates interfer- (after 10 SpO2 is running
ence detected secs.)
17 SpO2 probe off Probe off baby is SpO2 Probe Off 3 min 2 to 1 Primary Only available if
baby indicated from the Baby (after 10 SpO2 is running
Masimo board secs.)
18 Too much am- Masimo board Check SpO2 3 min 2 to 1 Primary Only available if
bient light indicates too much (after 10 SpO2 is running
ambient light secs.)
M1128927
able limits)
22 Callback timer Current callback Callback Timer See 2 Silencing this alarm will cause Primary
complete timer has reached Complete notes the timer alarm to shut off
target time
SpO2 Alerts
Rev. 02
1 Low perfusion Masimo board indi- Low Perfusion No No audio none Only active dur-
cates low perfusion silence ing alert condi-
tion
2 Low signal IQ Masimo board indi- Low Signal IQ No No audio none Only active dur-
cates low signal IQ silence ing alert condi-
alert tion
18 Too much Masimo board Check SpO2 No No audio none Only active dur-
ambient light indicates too much silence ing alert condi-
ambient light tion
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_______________________________________________________________________________________
gehealthcare.com
World Headquarters
EC Representative
GE Healthcare Datex-Ohmeda Ltd.
9900 West Innovation Drive Ohmeda House
Wauwatosa, WI 53226-4856 71 Great North Road
USA Hatfield Hertfordshire
Tel 1 800 345 2700 AL9 5EN
Tel +44 1707 263570
Fax +44 1707 260065
Brazil Only
GE Healthcare Clinical Systems Equipamentos Mdicos
Ltda
Av. Paulista, 37 - 13 andar
CEP: 01311-902 - Cerqueira Csar
So Paulo, SP - Brasil
Tel +55 11 3053 2500
Fax +55 11 3053 2573
Asia Representative
GE Healthcare
Maxdo Center No. 8 Xing Yi Road,
Hong Qiao Development Zone
Shanghai , China
Tel + 65 62773444