SPIN XS

Spin XS
Contents
1、SPIN XS Product Introduction
2、Analysis Principle and Method
3、System Parameter
4、Structure Characteristics
5、Liquid System
6、Electrical System
7、Optical System
8 、 Te s t P r o c e s s
9、General Operating Procedure
10、Maintenance
01 Product Introduction
The Auto Chemical Analyzer is mainly used for quantitative determination of serum,
plasma, urine, cerebrospinal fluid and other clinical biochemical items, therapeutic drug
concentration monitoring and drug of abuse monitoring.
Product description

1 SPIN XS Chemistry Analyzer constant speed conversion

The working cycle of reaction tray of the SPIN XS is 18 seconds. In one

working cycle, one sample is added by the sample probe, and within

1 hour(3600 seconds), 200 samples can be added, so it is a constant

speed of 200T/H.
Product description
2 Machine structure
• The auto chemical analyzer consists of a humanized software
operating system, precise optical unit, sophisticated mechanical
system, complex liquid system and highly integrated electronic
system.

3 Function
• The analyzer automatically completes the functions of sample
loading, reagent addition, stirring, reaction, heating, reaction
detection, cleaning, and calculation, display, printing of test
result. It completely mimics and replaces manual operation,
which not only improves work efficiency, but also reduces test
error. Improve the accuracy and speed of test results.
02 Analysis Principle and Method
Analysis Principle and Method

Lambert-Beer law

Lambert-Beer law is the basic law of spectrophotometry. The chemistry analyzer is based on the material

It describes the relationship between the intensity of selective absorption of light, analysis methods

light absorption at a certain wavelength and the that based on Lambert - Beer law.

concentration of light-absorbing substances and the

thickness of its liquid layer.

Analysis Principle and Method

⚫ Analysis principle ：
The specific wavelength of
monochromatic light through a
cuvette containing sample
solution, it is proportional that
intensity of monochromatic light
is absorbed (absorbance),
concentration of the sample
solution and distance light pass
through the solution(optical path).
Analysis Principle and Method
Lambert-Beer law ：

Among them:
Solution layer thickness (b), that is, the optical
• A - Absorbance is absorbed by solution.
path is fixed and known. Solution molar
• T - The Ratio of transmitted light intensity and incident light
intensity, transmittance. extinction coefficient (ε) is the wavelength, the
• I0 - Intensity of incident light. solution and the solution temperature
• It - Intensity of transmitted light. correlation coefficient, when the guaranteed

• ε - Molar extinction coefficient (ml × mmol-1 × cm-1). solution temperature stability, in its single
wavelength, the concentration of the solution
• c - Molar concentration of the solution (mmol/ ml).
and absorbance has linear relationship ( ε is
• b - Solution layer thickness (cm).
given directly in manufacturers reagent kit).
Analysis Principle and Method
Common analytical methods:
Endpoint method, Rate method and Fixed time method.

• End point method includes one-point end point method and two-point end point
method.

• Rate method is also called continuous monitoring method or kinetic method.

• Fixed time method is also called two-point rate method.

Analysis Principle and Method

End point method

Refers to the reaction after a period of time (usually a few minutes), the reaction proceeds
to completion, and all the substrates (test substances) are converted into products, which
is called the end point method.
Analysis Principle and Method
Rate method

It is used to continuously measure the multi-point data of the concentration of a

certain reaction product or substrate in the enzymatic reaction with time, determine
the initial velocity of the enzyme reaction, and indirectly calculate the enzyme activity
concentration.
Mainly used for the determination of enzyme activity.
Analysis Principle and Method
Fixed-time method

Selecting two photometric points. These two points neither measure the initial
absorbance nor the end absorbance. Calculate the difference between the
absorbances between the two points in a unit time for the calculation of the sample
concentration, called fixed time method (or two-point rate method).
03 System Parameters
System Parameters
Performance Standard
Speed 200T/H
Wavelength 340～800nm
Accuracy ±1nm
Basic Reaction Temp 37℃±0.1℃

Analysis Items Max 28 items together

Analysis Method End Point, Rate, Fix Time

Sample Position 37

Sample Serum, plasma, urine, CFS, etc.

Sample Sample Volume 2～70μl (0.1μl Step)
System
Sample&Reagent Probe Liquid level sensing, Remaining detection, Anti-collision function

Probe Washing Internal&external washing

System Parameters

Reagent Position 28

Reagent Volume 20～350μl(1μl Step)

Reagent Bottle
20mL, 50mL
Specification
Reagent
System Min Reagent 0.5mL(20mL bottle)/ 1.5mL (50mL bottle)

Sample&Reagent Probe Liquid level sensing, Remaining detection, Anti-collision function

Probe Washing Internal&external washing

Cooling Air cooling funciton

System Parameters
Cuvette Kind Discrete

Cuvette Qty 48
Reaction Time About 10 mins
Reaction Volume 120～500μl
Light Source 6V/10W Halogen Lamp
Abs Range 0～3.3Abs
Reaction System Accuracy 0.0001

Liner: K factor, 1-point, 2-point and multipoint.Non-Linear: Spline,

Calibration
Polygon, Index, Pgarithm, Logit-log4p, Logit-log5p.

Real time QC, Westgard multi rule, Cumulative sum check, Twin
QC
Plot(2D)
Auto Washing Auto washing sample probe, cuvettes

Mixing Speed adjustable stirrer with teflon coating.

System Parameters
Port TCP/IP Port

Data Processing Real time display reaction curve

Data System
Printer External, multiple reporting mode available

LIS System LIS system support

Net Weight 36Kg

External Sizer 625mm*425mm*460mm(W*D*H)

Analyzer
Power (VA) 300VA

Water Consumption 5-7L/H

Power Supply AC220V/AC110V,50Hz/60Hz

Installation&S
torage Storage: -10℃～40℃, ＜85%RH
Storage&Using
Working:15℃～30℃，35%RH～80%RH,Altitude:less than 2000m
04 Structure Characteristics
Structure Characteristics

• According to the structure classification of the reaction device, the Spin XS auto
chemical analyzer is discrete auto chemical analyzer.
• Discrete auto chemical analyzer: The chemical reaction of each sample to be tested
and the reagents are completed in the respective reaction cups.
• currently, most auto chemical analyzers are discrete structure that completely
imitate the manual process.
Structure Characteristics

Introduced from the following perspectives:

Instrument
Appearance System
cover internal Instrument
structure core structure
Structure Characteristics
Instrument appearance

1 2

Item Name Note

Protection loading system, detection unit, sample
1 Top cover
tray and reagent tray
Observation Can observe the working conditions of the internal
2
window sample loading system, detection unit, etc.

3 Front panel Use when maintaining the instrument

3
 Structure Characteristics
1

The power switch is located on the right side

4 Right side panel
panel
4 Turn the power and power cord connections
5 Power Board
on or off
5 6 Master power supply Instrument main control power switch
Refrigeration power
=
7 Power switch for the cooling section
supply
9
8 Switch Equipment operation switch
10

9 Fuse Safe operation of the protection circuit

6 7 8
Power input
10 Used to power the device
connector
 Structure Characteristics
Communication Connect the analyzer to the
11
Interface computer
Connected ground wire, pure water
12 L frame wastewater alarm, water
connection
13 Grounding bolt Connecting ground
11 13 12 Connect pure water and waste
14 Aviation joint liquid float level switch to realize
14
1
pure water and waste liquid alarm
Connect the snake skin tube and
15 Outlet
drain the waste liquid
Connect polyurethane hose to
16 water intake provide pure water for the
instrument
15
1 16
 Structure Characteristics
Instrument cover internal structure

Item Name Note

3 Reagent Place reagent bottles, sample cups, blood
1
&sample tray collection tubes, centrifuge tubes, etc.
6 2 Washing tank Cleaning reagent&sample probe or stirrer
Aspirate reagents and samples from the
2 3 Loading system reagent&sample tray and dispense them into the
5
reaction cup of the reaction system
1
4 Mixing system Stir the reagent and sample mixture in the cuvette
Reaction The reaction cup is fixed and the inside is kept at a
5
2 4 system fixed temperature to provide reaction conditions
Cleaning
6 cleaning the cuvette
system
Structure Characteristics
Instrument core 1 2 3 4 5 6 7 8 9

10 11 12 13 14 15 16

1-Piston pump | 2-Cleaning arm | 3-L frame | 4-Reaction tray | 5-Sample arm | 6-Washing tank
7-Reagent&sample tray | 8-Circuit board | 9-Power Board | 10-Miniature diaphragm pump | 11-Electromagnetic valve
12-Halogen lamp | 13-Optical path component | 14-Washing tank | 15-Mixing arm | 16-Power box
Structure Characteristics
Reagent&sample tray assembly
1

1-Sample position | 2-Reagent position

The reagent&sample tray is divided into sample position and reagent position,
sample position is 37, reagent position is 28.
Structure Characteristics
• The sample tube is used to hold the sample. Reagent&sample trays support different types sample tube.
Sample bits support the following sample container types:
• Micro sample cup:Φ12×37mm, 2ml
• Original blood collection tube or plastic test tube:
Φ12×68.5mm, Φ12.7×75mm, Φ13×75mm.
Structure Characteristics

• 20ml&50ml reagent bottle both available. One reagent position can put only one reagent bottle.
Specification and unavailable volume is listed below

Specification Dead volume

20ml 0.5ml
50ml 1.5ml

Please prepare enough reagents according to the minimum volume information above
Structure Characteristics
Cooling System

Reagent&sample tray refrigeration assembly

includes semiconductor refrigeration chip, heat
sink, cooling fan.

The semiconductor refrigeration chip has two faces,

hot and cold. When installing, pay attention to
recognize different faces.

The main component of the refrigeration control

system is the reagent&sample tray. The sample
reagent tray is kept at a low temperature for 24
hours through a cooling tray, a cooling fan, and a
heat sink.
Structure Characteristics
Reagent sample arm mechanism 1-Reagent&sample probe cover.
2-Ball spline shaft.
3-Sample arm main frame.
4-Left and right stepper motor.
5-Adapter plate.
6-Upper and lower stepper motor.
7-Reagent&sample probe-.
8-Left and right timing belt.
9-Up and down timing belt.
10-Bearing compression sleeve.
11-Pipe clamp.
12-Move up and down
Structure Characteristics
Reagent sample probe structure
Nut

Reagent&sample probe assembly includes: Up fixed screw

• Anti-collision probe holder, Spring
• Clamping sleeve
Adapter sleeve
• Spring
• Upper fixing wire Anti-collision base

• Nut
Structure Characteristics
Reagent sample needle function

➢ Aspiratting fixed amount of reagent or sample from the reagent sample tray and adding it to the reaction
cup.

➢ The sample probe has the function of detecting the liquid level in the sample container.

➢ The sample probe has an anti-collision function.

Structure Characteristics
Reaction system

Reaction system included reaction tray, reaction tray cover, reaction cuvettes, reaction thermostat.
Structure Characteristics
Reaction system

1-Reaction cuvette position, 2-Identification film,

5 3-Cover Gland, 4-Cuvette joint, 5-Cuvette
1

2 1

3
4 2

1-Fiber fixing hole, 2-Column

Structure Characteristics
4
Reaction system

1 5
2

3 6

1-Photoelectric switch, 2-Big Gear, 3-Fixed Base,

4-Axis, 5-Small Gear, 6-Step Motor
Structure Characteristics
Washing system 1-Washing Probe,
2-Linear guide slider mount,
3-Photoelectric switch,
1 6
4-Step motor,
7
5-Base of washing arm,

8 6-Compression screw for washing probe,

2 9 7-Fixed axis of washing probe,
3
8-Driven wheel,
9-Driven belt,
4 10
11 10-Up and down wheel,
5
11-Motor fixed board,
12 12-Fixed column.
Structure Characteristics
Cleaning system 4 5
• The reaction cup automatic cleaning system uses deionized water 1 2 3
to perform a 4-step automatic cleaning of the reaction cup to
ensure that the reaction cup is free from cross-contamination and
drying during the test

• The process of 4-step cleaning is as follows:

• First and second step wash the cuvette with deionized water.
• Third step to read water blank.
• Fourth step cleaning and wiping the cuvette.
Structure Characteristics
Mixing system
1
6
2

8
3

4 9
5

1-Probe Cover | 2-Stirrer | 3-Up&Down Base | 4-Up&Down Pulley | 5-Main Support | 6-Ball Spline Shaft,
7-Left&Right Pulley | 8-Left&Right Motor | 9-Up&Down Motor
05 Spin XS’ Fluidics
Spin XS Fluidics

BK-200mini structure
Spin XS Fluidicswaterway
scheme map
Spin XS Fluidics
Cuvette cleaning unit Halogen lamp

Pump
1

Valve 4 Valve 5

Pump Pump Pump

5 4 3
Spin XS Fluidics
Cleaning system Sampling Reagent
Stirring
cleaning plate
cup
cup condensate

Pump Pump Pump

5 4 3
06 Spin XS Electronics
Spin XS Electronics
Electrical scheme
Spin XS Electronics
Heating Reaction disk Reaction disk Pump valve
belt motor line photoelectric adapter plate
AD Module switch line interface

Black Waste
Black liquid(FY)
Red
Red Pure
ISO 1050 water(DI)
Communication
Temperature
chip
White control switch
Empty
Red Light blocking voltage

G LH V
adjustable
potentiometer
Communicati
700
on interface- Preamplifier voltage
A/D
— 4P conversi- measurement point
GND 578
communicati- on chip
on line
CPU B board
chip 510 interface
Red(K)

Black(M)
405

Halogen power 630

supply interface
546
A board
interface
450

340
GND-Black(B)
24V-Red(A)

Light blocking voltage and

AD board power post voltage measuring point
supply interface
Spin XS Electronics
The driving chip is driven from top to bottom in the order of: upper
and lower sampling arms, left and right sampling arms, plunger
pump, reagent sample tray, stirring arm up and down, stirring arm
left and right, cleaning armThe order of the lights from top to
bottom is: 1 D4, 2 D6, 3 D7, 4 D9, 5 D5,6 D8, 7 D10, when the
cover is in the limit position, the light is on, otherwise the light is Sample arm upper and
off. lower motor line（S1）

Drive Module Ground interface -

1
2
Sample arm upper and lower
photoelectric switch line
4P (4-pin) sample 3 （S1）
reagent arm 4 Sample arm left and right
adapter plate photoelectric switch line
（S2）
CPU-led running Sample arm liquid level
indicator - green: CPU line
chip
flashing light Sample arm left and
indicates that the right motor line（S2）
CPU chip is working Solenoid valve power
properly supply line (V1)
Piston pump motor line
(P)
ISO1050 Plunger pump photoelectric
Communication chip switch line (P)
Sample tray photoelectric
switch wire (T)
Sample tray motor
CPU-led running cable (T)
indicator - green: Stirring motor power
flashing light supply line
indicates that the CPU Mixing arm up and down
CPU chip is working chip motor line (J1)
properly Mixing arm up and down
photoelectric switch line
(J1)
Stirring arm left and
ISO1050 right photoelectric switch
Communication chip line (J2)
Mixing arm left and right
motor line (J2)
Cleaning arm motor
Communication
line (C)
interface - 4P
communication Cleaning arm
line photoelectric switch
wire (C)

Drive module power

supply interface
24V-Red(C) GND-Black(D)
Spin XS Electronics
Drive module—drive chip
The driving chip is driven
from top to bottom in the
order of: upper and lower
sampling arms, left and right
sampling arms, plunger pump,
reagent sample tray, stirring
arm up and down, stirring arm
left and right, cleaning arm.
The order of the lights from
top to bottom is: 1 D4, 2 D6,
3 D7, 4 D9, 5 D5,6 D8, 7 D10,
when the cover is in the
limit position, the light is
on, otherwise the light is
off.
Spin XS Electronics
Drive Module (Top half part)
Spin XS Electronics
Drive Module
(Down half)
Spin XS Electronics
D5：Speed, light is indicated as 100Mbps, and
Communication light off is indicated as 10Mbps

Red -A1
Black-B1
Communication board
D6：Connection indicator, the light is on to
power supply line
board module D1：Data transmission
indicate that the connection is normal
interface
indicator
D2：Data receiving
indicator
D3：IP address conflict Program debugging
D4：Full duplex (always interface
on) Network
port chip
D7 running
indicator - the
light flashes to
indicate that the D9 power indicator
CPU chip is light - light indicates
working properly. XBX-5NPCNB
that the 3.3V power
supply is normal.
CPU
chip
Network
port
Communication
interface, 12P
3 cable - detailed
1 2
wiring method
P3
ISO 1050 see line process
Communication
Rewrite mechanical chip
bit interface
Spin XS Electronics
Communication module — Rewriting mechanical position
The J1 interface is rewrite the mechanical bit interface. When you need to rewrite the mechanical position,
you can follow the steps below:

1. Disconnect the power cord first;

2. Place the shorting cap on pins 2 and 3 of the P3 interface.
3. After the power cable is connected, the D7 indicator—the green light flashes rapidly..
4. The short-circuit cap is removed and the instrument is initialized (the sequence of motion is
initialized as described above), that is, the rewriting of the mechanical position is completed.
5. After the mechanical bit is rewritten, the shorting cap can be placed at pins 1 and 2 of the P3
interface.

Note: The mechanical position rewrite, in addition to the mechanical position to restore the default
value, the level and stirring speed also return to the default value, need to be re-commissioned.
Spin XS Electronics
Pump valve adapter plate

XBX-BFZJ XBX-BFZJ

Note:
BB RB Pump 1 - Pump 5
V5 P5
line red and black
Gray
BB RB lines can not be
line V4 P4
V reversed,
BB RB otherwise the
V3 P3
pump will burn
out.
V2 P2 BB RB V——Valve
P——Pump
P1 B——Black
RB
R——Red
Spin XS Electronics
Level plate
Sampling needle signal line 1 This double-row pin

XSH-Ⅱ0205
2 is only used when
Note: downloading the
1 foot is connected to the program
shielded cable (black)
2 pin signal cable (red and Note: Do not insert
white) short circuit cap

DS1 (green light):

work indicator,
normal working
reagent level plate
flashes 2s
DS2 (red light): It
will be bright when
the liquid level is
detected, and it will
only be effective
after falling.

No. 2 FFC line interface

No. 1 FFC line interface

Spin XS Electronics
Adapter plate
XBX-CHC7 V2
Liquid level line
Line sequence:
green, empty, empty, blue

No. 2 FFC line

Liquid level line

Line sequence: No. 1 FFC line
red，white，black
07 Optical System
Optical System
The main components of the product light path system include:

• Halogen lamp（6V10W）
• Optical fiber
• Optical path assembly

A B

V
此处扎扎带
Optical System

Lens mount Halogen heat sink

Halogen lamp holder

Lens barrel

Halogen fixing plate

Semiconductor heat
sink

The light source adopts long-life light source, inclusive water cooling mode, average life of 2000 hours,
optimal position design, no moving parts, no signal attenuation, strong anti-interference ability.
08 Testing Process
Testing Process
Begin
Add sample
Initialization
Stir

Automatic cleaning
reaction cup Add R2 reagent Single reagent
longest reaction
reagent about
Determination of Stir 5.4min
water blank
End of full
metering
Reaction cup water
sucks dry
Automatic cleaning
reaction cup
Add R1 reagent
Automatic stop
Testing Process
Single and double reagent project test points
09 General Operating procedure
General Operating System

1. Check before operation, the power supply is well connected, the pure water is sufficient, the waste water tank is
emptied or the waste water drain pipe is smooth, the mechanical arms are in the initial position, and the disk cover
guide groove is positioned accurately.

2. Power on initialization until the instrument reaches the "standby" state.

3. Open the reagent bottle cap, load the reagents in the order of the reagents in the software, and scan the reagents to
confirm that the reagents are available on the same day.

4. Conduct quality control test, the quality control result is qualified within the target value range, and re-calibrate the
quality control (or modify the factor after quality control) until it is qualified.
General Operating System

5. Sample entry, start testing.

6. Review test results and print a report form.

7. After the work is finished, take out the reagent bottle, cover the reagent bottle in the order of the labeled bottle
cap, and put the reagent in a refrigerator with a constant temperature of 2-8 degrees or cover the reagent in the
reagent compartment.

8. Enter the instrument day maintenance, clean the needles of the instrument (clean with a cotton swab dipped in
cleaning solution from top to bottom).

9. Exit the software, turn off the computer, turn off the power to the instrument, and empty the waste water tank.
10 Maintenance
Maintenance

The maintenance items on the interface are divided into six cycles in the maintenance
cycle

• Daily: 1 day
• Weekly: 7 days
• Monthly: 31 days
• Every three months: 91 days
• Every six months: 181 days
• Other (not regular)
Maintenance
Daily maintenance
• A、 Cleaning the instrument table and the surface of each mechanism;
• B、 Check the waste water tank and empty the waste water tank every day.；
• C、 Clean the needle and unchoke if necessary;(using alcohol cotton swab)
• D、Check the washing tank if blocked; clean the cuvette.
Maintenance
Weekly maintenance
• A、 Clean the needle, the stirring needle and the cleaning needle with the cleaning solution, and
un-choke the needle if necessary.
• B、 Cleaning sample and reagent tray inside.
• C、 Wash the cuvette with a cleaning solution.
Maintenance
Monthly maintenance

A、 Clean the washing tank.

(using cotton swab with alcohol)
Maintenance
Every three months maintenance

• A、 Replacing the cuvette.

• B、 Cleaning the reaction tank.
Maintenance
Every six months maintenance
• A、Detect the instrument cleaning pipeline and decide whether it is necessary to replace the
pipeline according to the situation.
• B、Determine if you need to replace the light source depending on the situation.
Maintenance
Unscheduled maintenance
• A、Cleaning the instrument panel.
• B、Cleaning reagent&sample tray.
• C、Cleaning the reagent&sample probe inner wall.
• D、Replacing the reagent&sample probe.
• E、Replacing the stirrer.
• F、Replacing the cuvette.
Instrument Faults Handling
Instrument Failure Analysis Table:

Accident details Main reason Solution

The reagent&sample tip is dirty. Wipe the probe with a cotton swab dipped in an alkaline
Reagent&sample tip with water cleaning solution.
The pipe or filler of the sampling and filling
droplets Perform maintenance checks.
mechanism has leakage or full bubble.

Check the interface area and vent the water pipe.

The cleaning mechanism line leaks or is Perform maintenance on the cleaning mechanism.
Water drops on the cleaning
completely bubbled. If you need to replace the hose, please contact customer
needle
The nozzle and pipeline are blocked. service engineer.

No water flowing out of the 1. Carry out maintenance of the cleaning mechanism. If you
1. The nozzle and pipeline are blocked. want to replace the hose, please contact customer service
cleaning nozzle
engineer.
Instrument Faults Handling

1. The nozzle of the cleaning mechanism and the 1. Carry out maintenance of the cleaning mechanism. If you want
Water overflow in the cuvette to replace the hose, please contact customer service engineer.
pipeline are blocked.

1. The interface part is not properly installed. 1. Confirm the leak and reinstall it.
Syringe pump leakage 2. Replace the syringe pump.
2. Water leakage in the pump.

Confirm that the air enters and reinstall.

Perform exhaust in the system maintenance. If there are tiny
There are bubbles in the syringe 1. The interface part is not properly installed.
bubbles that cannot be removed, you can gently tap the syringe
pump 2. The filling device is not fully exhausted.
pump while the reagent or washing water is flowing, and use
vibration to eliminate it.

1. Poor contact of the level plate interface.

Check if the level plate interface line is in good contact.
2. There is a problem with the instrument
Abnormal liquid level detection Check if the grounding is connected.
grounding.
Check for large electromagnetic interference around.
3. There is a large electromagnetic interference.
 Instrument Faults Handling
Confirm that the reagents are prepared and placed in the correct position.
Check for impurities in the sample.
Absorbance exceeds The absorbance of the reaction solution exceeded
Check the reaction tank for water or impurities.
upper or lower limit the range of 0 to 3.3 Abs.
Inspect the cuvette for cracks and scratches.
Check that the optical window is clean or ingress.

Stop the test after the The sample and reagent&sample probes have an anti-collision function.
instrument is abnormally a striker occurs. When the probe is hit, the machine needs to be restarted. After the position
cleaned check is adjusted, the test is restarted.

Confirm that there are no foreign objects at the code teeth and
1. The reaction tray cannot find the stop position.
photoelectric switches below the reaction disk.
Reaction tray abnormality 2. The reaction tray does not stop at the specified
Check if the photoelectric switch and motor wiring are disconnected or
position.
abnormal contact.

Check if the photoelectric switch cover is abnormal.

1. The movement in the left and right direction is
Check if the corresponding photoelectric switch and motor wiring are
Reagent&sample probe abnormal.
abnormal.
position abnormality 2. The movement in the up and down direction is
Check if there is any abnormality in the corresponding drive board
abnormal.
installation.
 Instrument Faults Handling

Check if there is any abnormality between the heater wire and

the circuit board wiring.
Abnormal reaction tray temperature 1. The temperature of the reaction disk is abnormal. Check if the temperature control probe is installed properly.
The temperature is adjusted by software.
Observe how the board works.

1. Confirm that there is no abnormality in the optocoupler on the

lower side of the reagent&sample tray.
2. Check if the optocoupler and motor wiring are off or
1. The reagent&sample tray is abnormally moved.
abnormal.
Reagent&sample tray abnormality 2. The reagent&sample disk does not stop at zero
3. The reagent&sample tray is loose.
when it is initialized.
4. The calibration position of the reagent&sample tray is
unreasonable, and the zero position should be within 90 degrees
of the reagent&sample probe level.
 Instrument Faults Handling
1. The instrument is not properly maintained on a 1. Regularly maintain the instrument in accordance with the user
regular basis. manual.
2. The reagents deteriorate and there are chemical 2. Replace the new reagent and properly store and use the
substances or impurities. reagent.
3. The quality of pure water is poor. 3. The conductivity of pure water should be below 1μs/cm.
4, cleaning is not complete. 4. Wash the reaction cup thoroughly with the cleaning solution.
Poor repeatability 5, the reagent crystallizes 5, replace the reagent
6. Analyze cross-contamination between projects. 6. Place reagents that may be cross-contaminated or use a cross-
7. The sample is unqualified (fibrin in the sample). contamination procedure to avoid them.
8. There is a large electromagnetic interference. 7. Centrifuge the unqualified sample again.
8. Remove the interference source.

The calibrator is used immediately after it is added to the sample

The calibrator is concentrated or ineffective.
Poor accuracy cup and stored correctly.
Poor analysis condition setting.
Set the parameters correctly.

No response after the instrument is Poor contact of the power plug Detect the power input part wiring
turned on Instrument fuse burned out Replace the fuse and check the line
Thank you very much