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Contents
CONTENTS
CHAPTER 1
INSTRUMENT INTRODUCTION.......................................................................... 1
1.1
STRUCTURE ..........................................................................................................................1
1.1.1
Host .......................................................................................................................................1
1.1.2
Accessory ..............................................................................................................................1
1.2
PURPOSE................................................................................................................................2
1.3
SPECIFICATIONS ..................................................................................................................3
1.4
STRUCTURE ..........................................................................................................................7
1.4.1
Front Panel.............................................................................................................................7
1.4.2
Rear panel..............................................................................................................................7
1.5
OPERATION ...........................................................................................................................9
1.5.1
Display Screen.......................................................................................................................9
1.5.2
Menu......................................................................................................................................9
1.6
1.6.1
1.6.2
1.6.3
1.6.4
CHAPTER 2
HARDWARE............................................................................................................ 16
2.1
CPU BOARD.........................................................................................................................16
2.1.1
Function...............................................................................................................................16
2.1.2
Interface...............................................................................................................................17
2.2
2.2.1
Function...............................................................................................................................17
2.2.2
2.3
2.3.1
Function...............................................................................................................................19
2.3.2
Interface...............................................................................................................................19
3.2.3
HGB Unit.............................................................................................................................24
3.2.4
V1.0
Contents
3.2.5
3.2.6
Auxiliary Unit......................................................................................................................24
4.1.3
4.1.4
4.1.5
4.1.6
Disassemble/Replace Chamber............................................................................................29
GENERAL.............................................................................................................................31
5.2
5.3
ROUTINE MAINTENANCE................................................................................................33
6.1.1
6.1.2
Replace Fuse........................................................................................................................34
6.2
6.3
6.4
6.5
YEARLY MAINTENANCE..................................................................................................35
INSTRUMENT THAT
TROUBLESHOOTING .......................................................................................... 37
7.3
BACKGROUND CHECK.....................................................................................................38
II
T- 6807-30-02357
V1.0
Instrument Introduction
Chapter 1
1.1
INSTRUMENT INTRODUCTION
STRUCTURE
1.1.1
Host
Control the process of sample collection, dilution and analysis, including the following units:
Hematology analyzer
RBC chamber
CCU board
Dilution machine
CPU Board
System software
Vacuum pump
block
Power supply
Dilution block
Sample machine
1.1.2
WBC chamber
TFT cable
Glass bulb
Adapter PCBA
Switch parts
Backboard parts
Transformer
Liquid tubing
Liquid Sensor
Accessory
Instrument Introduction
waste cap components;
3. PS232 Communication cable;
4. Waste barrels;
5. Printer (Optional ), Bar code scanner (Optional )
1.2
PURPOSE
It is used for detecting the parameters of RBC, WBC, HGB and differential counter.
The analyzer is used for the determination of the following 20 parameters and 3 histograms blood
specimens in Table 1-1.
Item
Abbreviation
Unit
WBC
109/L
Lymphocyte
LYM#
109/L
Mid-sized cell
MID#
109/L
Granulocyte
GRAN#
109/L
Lymphocyte percentage
LYM%
MID%
Granulocyte percentage
GRAN%
RBC
1012/L
Hemoglobin Concentration
HGB
g/L
Hematocrit
HCT
MCV
fL
MCH
pg
MCHC
g/L
RDW-SD
fL
RDW-CV
Platelet
PLT
109/L
MPV
fL
PDW
Plateletcrit
PCT
P-LCR
WBC Histogram
RBC Histogram
Platelet Histogram
PLT Histogram
Table 1-1
Instrument Introduction
1.3
SPECIFICATIONS
Principles of Measurement
Blood Cells are counted and sized by Electrical Impedance Method. Hemoglobin is
determined by Colorimetry Method.
Parameters of Measurement
Basic parameters:
Item
Abbreviation
Unit
WBC
109/L
RBC
1012/L
Hemoglobin Concentration
HGB
g/L
Platelet
PLT
109/L
Abbreviation
Unit
Lymphocyte percentage
LYM%
MID%
Granulocyte percentage
GRAN%
Instrument Introduction
Mean Corpuscular(erythrocyte) Volume
MCV
fL
RDW-SD
fL
RDW-CV
MPV
fL
PDW
P-LCR
Deviation
Red Blood Cell(erythrocyte) Distribution
Width Coefficient of Variation
Calculated Parameters:
Item
Abbreviation
Unit
Lymphocyte
LYM#
109/L
Mid-sized cell
MID#
109/L
Granulocyte
GRAN#
109/L
Hematocrit
HCT
MCH
pg
MCHC
g/L
Plateletcrit
PCT
Sampling Features:
Venous and Capillary Blood Mode:
Prediluted Mode:
WBC/HGB
RBC/PLT
1:44600
WBC/HGB
1:355
RBC/PLT
1:44500
80m
Display
Liquid Crystal Display (LCD),resolution:640480
Language
1:300
Instrument Introduction
English
Indicator
20 Parameters and 3 Histograms Display
Alarm Indicator
Working Status (including Power Supply) Indicator Light
Alarm
Interface
One power input socket
One printer port
One VGA display port
Two RS232/C serial ports
Two USB interfaces
Two PS/2 interfaces
Recorder
Rapid Thermal Recorder
Recording width:
48mm
Paper width:
57.5mm
When the liquid reagent is in the sensor the voltage is 3.0V ~ 5.0V;
When the liquid reagent is not in the sensor the voltage is 1.5V
WBC Aperture voltage reference valuethe 5 times average W.H.V.S value of blank test
RBC Aperture voltage reference valuethe 5 times average R.H.V.S value of blank test.
Aperture voltage
Press T1
Press T2
Take electrode cable from CCU board and use the two pens of multimeter (which
5
Instrument Introduction
have been set the resistance value) to measure the Chamber shield and substrate
Insulation. The value should be more than 20MWhen you finish test, return the
electrode cable back. The value should less than 1
Parameter Range
Parameter Range
WBC
0.0 - 99.9x109/L
GRAN#
0 - 99.9x109/L
RBC
0.00 - 9.99x1012/L
HCT
0.0 - 100.0%
HGB
00.0 - 300g/L
MCH
0.0 - 999.9pg
PLT
0 - 3000x109/L
MCHC
0.0 - 999.9g/L
MCV
0 - 250fL
RDW-SD
0.0 - 99.9 fL
LYM%
0 - 100%
RDW-CV
0.0 - 99.9%
MID%
0 - 100%
PDW
0.0 - 30.0%
GRAN%
0 - 100%
MPV
0.0 - 30.0fL
LYM#
0 - 99.9x109/L
PCT
0.0 - 9.99%
MID#
0 - 99.9x109/L
P-LCR
0.0-99.9%
Operating Ambient
Temperature:
15~35
Humidity:
10~90%
Atmospheric Pressure:
86.0kPa ~106.0kPa
Ambient Storage
Temperature:
-10~40
Humidity:
80%
Atmospheric Pressure:
Parameter
50.0kPa ~106.0kPa
Electric Specifications
Power Supply:
AC 100-240V,
501Hz,
AC 250V
2A
Instrument Introduction
394mm381mm500mm
Weight:
23kg
1.4
STRUCTURE
1.4.1
Front Panel
Figure 1-1
1. Power Light
2. [START] Key
3. Sample Needle
4.Display Screen
5. Thermal Recorder
1.4.2
Rear panel
Instrument Introduction
5
4
6
2
7
3
18
17
16
15
14
13
12
1110
chart 1-2
1. Equipotentiality
4. Printer Interface
9. Air Filter
Instrument Introduction
1.5
OPERATION
1.5.1
Display Screen
INFORMATION
SECTION
SECTION
SHORTCUT KEY
SECTION
1.5.2
Menu
You can operate the instrument by menu. Press the right key of the mouse, directing to the
function menu of the current window. Move the mouse to the required menu bar, and then press
the left key of the mouse, the required function will be selected. Pressing the left key out of the
9
Instrument Introduction
menu area, the operation will be canceled.
The common functions are showed at the top right corner of the screen as shortcut key. Move the
mouse to the function you wanted.
The menu functions are as follows:
Sample Mode: Choose the sample mode among Venous Blood Mode, Capillary Blood Mode and
Prediluted Mode.
Diluent: Inject the diluent quantificationally by sample needle. This menu uses only in Prediluted
Mode.
Information: Enter the information window of the next sample, input and modify the
information.
Histogram: Enter the histogram adjustment window of the current sample. You can manually
adjust the histograms of the current sample.
Print: Output the data of the current sample to the appointed device.
Function: Enter the function menu.
Mute: Stop the alert.
Help: Access the system help window.
About: Display information of the instrument such as software and copyright etc.
Shutdown: Startup the shutdown program to rinse the measurement unit automatically. Shutoff
the power supply when the screen displays Please switch off.
Function Menu
Review: Enter the review window. You can review, inquire or modify the measurement data of the
former sample.
Calibration: Enter the calibration window to calibrate the instrument.
Quality Control: Enter the quality control window to carry out quality control operation.
Setting: Enter the setting menu.
Service: Enter the service menu.
Calibration Menu
Manual Calibration: Enter the manual calibration window to calibrate the instrument manually.
10
Instrument Introduction
Auto Calibration: Enter the auto calibration window to adjust the instrument automatically.
QC Menu
QC Edit: Enter the QC edit window to edit the QC parameters.
QC Run: Enter the QC run window to carry out the selected QC files.
QC Graphs: Enter the QC graphs window to browse the selected QC graphs.
QC Table: Enter the QC table window to browse the selected QC tables.
Setting Menu
Time: Enter the time setting window to set the time of the instrument.
Printout: Enter the printout window to set the functions such as print or report.
Config: Enter the config window to set the functions such as print, sleep, clean, and display etc.
Limits: Enter the limits window to modify the limits.
Department: Enter the department window to set the department and abbreviation.
Operator: Enter the operator window to set the department, abbreviation, department and
operator.
Service Menu
Flush: To get rid of the aperture clog.
Enhanced Flush: To get rid of hard aperture clog.
Cleaning: Run the normal rinse process to rinse the measurement unit.
Enhanced Cleaning: Rinse the measurement unit with RINSE.
Drain Chambers: Empty the liquid of the counter pool.
Park: Run the Park Program to rinse and empty the tubing.
Prime Diluent: Inject the Diluent to the appointed tubing.
Prime Lyse: Inject the Lyse to the appointed tubing.
Prime Rinse: Inject the Rinse to the appointed tubing.
Instrument Introduction
Special: Enter the Special window to maintain the instrument.
1.6
DETECTION PRINCIPL
1.6.1
The count principle of the instrument is based on the measurement of changes in electrical
resistance produced by a particle passing through an aperture sensor.
a) The sample blood is diluted in a conductive liquid. As blood cells are non-conductive, the
diluent is a good conductor. There are big differences between them.
b) When the diluent passes through the aperture sensor, electrodes are submerged in the liquid on
each side of the aperture to create continuous current.
c) When cells pass through the aperture, the resistance between the electrodes increases as the
cell volume increasing, as is shown in figure 1-4.According to the Ohm Formulary: U=RI
(U=Voltage I=Current R=Resistance).If
increasing.
d) Passing through the magnification circuit, the voltage signal will be magnified and the noise
will be filtered, then you will gain the analytical results, as shown in figure 1-4.
e) One count pool and the detection circuit count the WBC. Another count pool and the detection
circuit count the RBC and PLT. The microprocessor of the instrument calculates and analyzes
the cells (WBC, RBC, PLT), and then gives out the histograms.
f)
PLT count adopts advanced liquid, electronics and software system. It settles the repetitive
count of the cells on the side of the aperture count area.
12
Instrument Introduction
Figure 1-4
1.6.2
Adding lyse in the blood, the red blood cell will rapidly be broken down and release hemoglobin.
Hemoglobin and lyse form a new mixture, which can absorb the wavelength of 540nm.Measure
the absorbency. Through the comparison of the absorbency between the pure diluent and the
samplethe concentration of the sample hemoglobin is calculated.
1.6.3
When different types of cells pass through the aperture sensor, there will be different electrical
pulse height. Because of the evident difference of the cells sizes, the instrument is able to
differentiate the white blood cell, red blood cell and platelet by its pre-set program.
The volume distributions are as follows:
WBC
1201000fL
RBC
8298fL
PLT
235fL
The leucocytes disposed by lyse can be divided into three types, according to their volumes:
lymphocyte (LYM), mid-sized cell (MID), Granulocyte (GRAN).
LYM
MID
3590 fL
90160 fL
13
Instrument Introduction
GRAN
1.6.4
160450 fL
The parameters of the sample blood test can be described in three ways:
a) Measured directly, such as WBC, RBC, PLT, HGB.
b) Derived from histograms, such as LYM%, MID%, GRAN%, MCV, RDW-SD,
RDW-CV, MPV, PDW, P-LCR.
c) Calculated, such as LYM#, MID#, GRAN#, HCT, MCH, MCHC, PCT.
The derivation of the formularies as follows:
z
MCV derives from histograms and the instrument collecting and classifying the
erythrocytes according to its volume. It is determined by measuring the average volume
of individual erythrocytes, and the unit is fL.
RDW represents the volume distribution of the erythrocyte populations, derived from
the RBC histogram. It can be expressed by the coefficient variation of the erythrocyte
volume as RDW-CV, and the unit is %.It can also be expressed in standard deviation of
the erythrocyte volume as RDW-SD, the unit is fL.
MPV is the average volume of individual platelets, derived from the PLT histogram. It
represents the mean volume of the PLT populations and can be expressed in fL.
PDW derives from the PLT histogram. It represents the geometry standard deviation (10
GSD) of the volume of the PLT populations.
P-LCR derives from the PLT histogram. It represents the ratio of the larger PLT and the
unit is %.
14
HCT(%)= RBCMCV/10
MCH(pg)= 10HGB/RBC
MCHC(g/L)= 100HGB/HCT
PCT(%)= PLTMPV/10
Instrument Introduction
z
15
Hardware
Chapter 2
HARDWARE
2.1
CPU BOARD
2.1.1
Function
With CPU as the core, the computer system also includes some peripheral equipments, such as
DRAM, SRAM, besides there are some interfaces, such as USB interface, COM2 interface,
COM1 interface, LPT printer interface, power supply interface, mouse/keyboard interface, display
screen TFT cable interface, peripheral display interface, DOM interface. As the chart 2-1.
The basic components of the computer system are CPU, DRAM, SRAM. They also supplied the
basic running environment for software.
16
Hardware
2.1.2
Interface
1 COM1interface
2 COM2 interface
3 USB interface
4 Mouse interface
3
5 Keyboard interface
6 Display
TFT
cable
interface
7 VGA external display
interface
4
5
6
7
Chart 2-1
2.2
CCU BOARD
2.2.1
Function
2.2.2
Analog/Digital converted
Analog Circuit
Circuit
HGB Measurement Circuit
Front Interface
17
Hardware
1
5
Chart 2-2
18
Hardware
10
11
Chart 2-3
1. Cpu Interface
2.
4.
Valve Interface
6.
10.
2.3
2.3.1
Function
The function of TFT Cable Converting Board is to connect all blocks and CCU board, and to
adjust the sensitivity of liquid sensor through adjusting the trimmer on TFT Cable Converting
Board.
2.3.2
Interface
19
Hardware
Adjustable potentiometer
Valve jack
Chart 2-4
20
Hardware
Power
supply
interface
Chart 2-6
Drawing tablets
DOM jack
Drawing tablets
Chart 2-7
21
Tubing
Chapter 3
TUBING
Chart 3-1
22
Tubing
3.2
1
7
2
4
4 Dilution sensor.
5 Waste liquid sensor.
6 Dilution block
7 Sample machine.
8 Glass bulb
9 Cleaner sensor.
3.2.2
Chart 3-2
The instrument includes four tubing sensor: diluent tubing sensor, rinse tubing sensor, lyse tubing
sensor, waste liquid sensor and reagent temperature sensor.
The tubing sensor, rinse tubing sensor, lyse tubing sensor are sued to check if the reagent enters
into the tubing system. If there is no reagent in the tube. The instrument will give alarm of no
diluent or no cleaner or no lyse.
Waste liquid sensor is used to test if the waste liquid is full. If yes, there instrument will give alarm
of waste liquid full.
reagent temperature sensor is used to check the reagent temperature in the tube. If the temperature
is too low the instrument will give alarm of temperature too low.
23
Tubing
3.2.3
HGB Unit
3.2.4
Dilute Unit
This part consists of sample sucker structure and dilution structure. Sample sucker structure is
used to aspirate sample, add it into the probe structure and clean the sample needle. Dilution
structure is used to provide power to suck sample.
3.2.5
Vacuum Unit
3.2.6
Auxiliary Unit
This part mainly refers to the tubing hose, connecting tube and electromagnetically operated
valve.
24
System Structure
Chapter 4
SYSTEM STRUCTURE
slider
Chart 4-1
25
System Structure
It is necessary to replace the sample needle wipe block, seal washer and synchronous driving belt
of the sample machine periodically. The replacing cycle is one year.
4.1.2
4.1.3
26
System Structure
4.1.4
It is necessary to replace the seal washer of the vacuum pump periodically. The replacing cycle is
one year.
27
System Structure
4.1.5
It is necessary to replace the seal washer of the piston block periodically. The replacing cycle is
one year.
28
System Structure
4.1.6
Disassemble/Replace Chamber
Chart 4-6
29
System Structure
Chart 4-7
30
Adjustment
Chapter 5 ADJUSTMENT
This part introduces how to adjust the gain of the passage.
5.1
GENERAL
5.1.1
31
12
32
Maintenance
Chapter 6
MAINTENANCE
As other precision instrument, only careful daily service and periodic maintenance can the
instrument have a good working status, and can we get the reliable measurement results and have
less malfunctions. This chapter introduces some preventive methods for service and maintenance.
If you want to know more relative information, please contact the customer service department of
Procan.
According to the requirements for maintenance of the instrument during the using procedures, we
divide the preventive service and maintenance into the following types: daily, weekly, monthly,
yearly and maintenance according to actual need.
Warning:
If the hospital or agency dont perform a satisfying plan to maintain the instrument, there
will be abnormal malfunction.
6.1
ROUTINE MAINTENANCE
6.1.1
Wipe the appearance of the instrument with neutral detergent or distilled water.
Caution:
Avoid using corrosive acids, alkali, and volatile organic solvent such as: acetone, aether,
chloroforms to wipe the appearance of instrument. Only can use the neutral detergent.
Caution:
Avoid wiping the inner of the instrument.
33
Maintenance
6.1.2
Replace Fuse
The fuse is installed in the fuse-box on the side of power switch. Open the box to replace the fuse
expediently.
Appointed specification fuse: AC 250V 2A
Warning:
Only can use the appointed specification fuse.
6.2
DAILY MAINTENANCE
it can
instrument in good working status. Set the auto cleaning procedure according to the
section 6.3. The general setup principles are:
Working time > 8 hours, auto-cleaning time=8 hours;
4 hours<Working time<8 hours, auto-cleaning time=4 hours;
Working time< 4 hours, auto-cleaning time=2 hours
The auto-cleaning time will decrease 1 hour year by year.
Shutdown
The instrument should be operated by auto maintenance before shut off the instrument.
You only need to clean the workbench and wipe the appearance of instrument when the
power-off.
6.3
WEEKLY MAINTENANCE
This instrument has installed weekly maintenance procedure. Act as follows:
a) Prepare E-Z cleanser and probe cleanser.
b) In the main operation window, press the right key of the mouse, pops up the menu.
34
Maintenance
In the menu area, select Service/Maintenance. Operate as the screen shows.
c) Turn off the power supply.
d) Wipe the appearance of instrument as section 6.1.1.
6.4
MONTHLY MAINTENANCE
It is necessary to clean the dust of the instrument monthly.
Operate as follows:
a)
Turn off the power supply, and pull out the power line.
b)
Take off the cover and the net. Clean them with neutral detergent brush and put them in the
shade.
c)
Airing naturally .Brush away the dust clinging on the air filter grid at the rear panel of
instrument.
d)
Put the air filter grid on the air filter net carefully. Planish them.
Notice:
Only can use the neutral detergent cleaning the air filter. Avoid airing it with heat.
6.5
YEARLY MAINTENANCE
Its necessary to perform preventive maintenance once every year. Because of the
highly-requirements for yearly maintenance, the maintenance should be performed by the
authorized engineer of Procan. Please contact the customer service department of Procan before
yearly maintenance.
6.6
THE
MAINTENANCE
BEFORE
TRANSPORT
OR
FOR
In the main operation window, press the right key of the mouse, choose Service/Park
35
Maintenance
in the menu.
b)
c)
Rotate the bottle covers of rest reagents and store them as the reagent operation
introduction. User should perform efficient action to prevent the material from
deteriorating, mis-eating and misusing.
d)
Plug the stopples which were pulled out at the first installation into the corresponding
tube connector.
e)
Pull out diluent connection tube, rinse connection tube, lyse connection tube and waste
connection tube and clean them with distilled water. Dry them in shady place, then
packing them into plastics.
36
f)
Pull out the power wire, packing it in plastics after cleaning with neutral detergent.
g)
Put the instrument and parts packed in plastics into packing cases.
Troubleshooting
Chapter 7
TROUBLESHOOTING
Start
instruments,
observation
self-test
Start up abnormal
equipment
is
normal,
NG
abnormalities,
Liquid
road
system leakage
OK
Blank
Test
Mainten
ance
all
technical
requirements
Maintenan
NG
does
or
not
technical
not
meet
the
requirement
--- High
OK
Make sure the
reagent
is
connected correct
and reliable
Sample test
The test result is
steady or not (CV
value is accord with
NG
Sample tests do
not
meet
technical
Maintenance
technical
requirement
OK
END
Chart 7-1
37
Troubleshooting
7.2
1535
1090%
86.0kPa106.0kPa
If the temperature is below 15,the activity of the reagent will reduce. It will weaken the capacity
of dissolving the blood. In a certain time, it can not break down the red blood cell membranes into
2fl cellular debris. At lower temperature conditions, the red blood cell debris will gather together.
It will affect the measurement of leukocyte, resulting in the count value of WBC increasing .It will
also affect the measurement of HGB, resulting in the count value of HGB increasing.
Checking for Sample Blood
Sample Collection: Observe whether the operator uses correct method to collect the blood
(Operating as PE-6800 FULLY AUTO HEMATOLOGY ANALYZER OPERATION MANUAL
/Chapter 3/Section 3.5 Preparation For Sample Collection), and whether the sample is stored in
the container filling with EDTA.K2O.H2O anticoagulant.
Sample Storage: After the sample blood is well-mixed, test on the instrument promptly. As time
goes by, the volume and density of the cells will change. The environment and the patient
determine the varying rate of the volume and density. If the sample is placed a long time at room
temperature, the volume of RBC will increase, and the MCV, RDW, PDW will be affected, and the
PLT will easily gather together.
Affection of WBC Classification: To get the exact measuring results, the venous blood sample
measurement must be completed within 4 hours. If the sample blood is placed a long time at room
temperature, the total number of WBC may change little, but the classification is inaccurate.
7.3
BACKGROUND CHECK
Background Check: This item can ensure the measurement and the calculated data wont be
affected by reagent empty. If the background value exceeds the permissive area, the measured and
calculated data will be inaccurate.
The permissive range of the background test results is
38
Troubleshooting
Parameter
Background Range
Unit
WBC
0.2109/L
109/L
RBC
0.021012/L
1012/L
HGB
1g/L
g/L
HCT
0.5
PLT
10109/L
109/L
Background Test Method: When power-on, suggested to run background test, you can also
execute background test as you need.
The operation steps are as follows:
a)
In the blood cell analyzer window, press Info button, and pops up the information
edit window. Then click the item textbox, change the ID as 999999999.then press
OK, return to blood cell analyzer window.
b)
Background count in venous or capillary mode, press the START key below the
sample needle directly for background count. In prediluted mode, the sample needle
aspirates some non-contaminated diluent from the chamber for background count.
The diluent pick-up method as follows(Analyzing the sample in prediluted mode, it
is also necessary to dilute sample with the diluent which is prior picked-up in this
method):
In main operation area, press the right key of the mouse, pops up the menu. In menu operation
area, select Sample Mode/ Prediluted to set the sample mode as prediluted mode.
In main operation area, press the right key of the mouse, pops up the menu. In the menu operation
area, select Diluent. Place a clean empty chamber or tube under the sample needle, press
START key to dispense the diluent into the chamber. Press the START key once, the diluent
is dispensed into the chamber or tube once (The quantity can be used for background count in the
second prediluted mode).
Press Exit button to return to the main operation area.
Affected Factors of Background:
1
39
Troubleshooting
3
Electronic interference affects measurement and the calculated circuit, for example:
Interference created by voltage fluctuation, peripheral equipment such as centrifugal
machine, CT machine, magnetic resonance device, etc.
40
Tubing Contamination
Lead label
Stick place
Label name
note
Motor A
MA
Motor B
MB
Motor C
MC
Dilution monitor
Motor D
MD
Optocoupler A
OSA
Optocoupler B
OSB
Optocoupler C
OSC
Dilution switch
Optocoupler D
OSD
Dilute sensor
DLS
10
Lyse sensor
LYS
11
Cleaner sensor
CLS
12
Waste liquid
sensor
WST
13
switch
STA
14
MTB board
MTB
15
valve
V1.V2V16
41
No: F-6807-30-02301
Temperature
Edition
Humidity
Requirement
Result
OK
Not ok.
OK
Not ok.
Display screen
OK
Not ok.
Mouse interface
OK
Not ok.
Keyboard interface
OK
Not ok.
Indicator light
OK
Not ok.
Reagent alarm
OK
Not ok.
OK
Not ok.
OK
Not ok.
valve
OK
Not ok.
OK
Not ok.
V
appearance
fitting
Backboard fan
Data circuit
Adjust to 4.31V
Burning function
OK
Not ok.
Motor
associated
parts
OK
Not ok.
OK
Not ok.
and
moving
Negative pressure of
vacuum chamber
79.21 KPa
Vacuum
leak rate
chamber
42
5.000.5V
KPa
KPa /2Mins
V
Note
Air Mixer
The
ability
of
chamber
shield
(cover) and the
substrate insulation
Less than3V
ml
OK
Not ok.
OK
Not ok.
Lymphocyte peak
fL
RBC peak
fL
WBC
0.2109/L
0109/L
RBC
0.021012/L
01012/L
HGB
1g/L
0g/L
HCT
0.5
OK
Not ok
0
9
1010 /L
0109/L
12S+1S
920V
8.00.4ml
PLT
up
Click
down
Aperture
voltage
Channel gain
OK
Not ok
WBC
RBC
The
average of
blank test
result
The
average
value of 5
times
counting
time
Every time
of blank
test
is
ok.
OK
Not ok.
WBC
200KB
OK
RBC
100KB
Not ok.
Any
blank
43
one
test
Carrying
contamination test
Instrument
calibration
PLT
300KB
WBC
0.5
RBC
0.5%
OK
HGB
0.5%
Not ok.
PLT
Venous
and
Periphera
l blood
calibratio
n
paramete
r
1.0%
WBC
RBC
HGB
MCV
OK
Not ok.
OK
Not ok.
Pre
dilute
calibration
parameter
Accuracy testCV
Test accuracy
result
PLT
WBC
RBC
HGB
MCV
PLT
3.0%
3.0%
3.0%
1.0%
7.0%
WBC accuracy
error range
6%
RBC accuracy
error range
5%
HGB accuracy
error range
4%
MCV accuracy
error range
5%
PLT accuracy
error range
14%
OK
Not
ok.
Venous blood
Predilution
model
model
OK
Not
ok.
OK
Not ok.
are alarm.
Pinter and net
function
WAperture
estimation.
44
Not ok.
OK
Not ok.
Troubleshooting
Possible Reason
Troubleshooting
Abnormal
background test
Electronic interference
Tubing contamination
Aperture clogs
Inadequate diluent
MTB is broken
Bubbles
Clogs
Unclear display
Abnormal
HGB
background
voltage
supply
45
Troubleshooting
Liquid leaks
Measure
minutes
Reagent is used up
No reagent,
Rinse(diluent/lyse)
empty alarm
Reset the
Aperture
There is no result
of
Abnormal
mid-sized
percentage
cell
RBC,
WBC
the
sample
reference
within
voltage
30
of
measurement
46