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V13 - 00 Technical Manual H18-Ant2
V13 - 00 Technical Manual H18-Ant2
1. SPECIFICATIONS......................................................................... 15
1.1. FRONT FACE VIEW 15
1.2. BACK PANEL VIEW 16
1.3. SYSTEM SPECIFICATIONS 17
1.3.1. PARAMETERS 17
1.3.2. VOLUMES 18
1.3.3. DILUTION 18
1.3.4. INPUT/OUTPUT 18
1.3.5. PRINTOUT 18
1.3.6. LINEARITY AND PRECISION 18
5. ELECTRONICS ............................................................................. 39
6. MECHANICS ............................................................................... 50
6.1. SAMPLE PROBE ARM 50
6.1.1. ITEM CODE: S020062-02 50
6.1.2. FUNCTION 50
6.2. DILUTION MACHINE 51
6.2.1. ITEM CODE: S020023 51
6.3. VACUUM PUMP MACHINE 52
6.3.1. ITEM CODE: S020064 52
9. MAINTENANCE ........................................................................... 72
9.1. USER MAINTENANCE 72
9.1.1. DAILY MAINTENANCE 72
9.1.2. WEEKLY MAINTENANCE 72
9.1.3. ON DEMAND MAINTENANCE 72
9.1.4. MAINTENANCE LOG 73
9.2. SFRI TECHNICAL MAINTENANCE 75
9.2.1. PREVENTIVE MAINTENANCE PROCEDURE 75
SFRI Sarl owns all rights to this unpublished work and intends to maintain this work as confidential.
SFRI Sarl may also seek to maintain this work as an unpublished copyright. This publication is to be
used solely for the purposes of reference, operation, maintenance, or repair of SFRI Sarl equipment.
No part of this can be disseminated for other purposes.
In the event of inadvertent or deliberate publication, SFRI Sarl intends to enforce its rights to this work
under copyright laws as a published work. Those having access to this work may not copy, use, or
disclose the information in this work unless expressly authorized by SFRI Sarl to do so.
All information contained in this publication is believed to be correct. SFRI Sarl shall not be liable for
errors contained herein nor for incidental or consequential damages in connection with the furnishing,
performance, or use of this material. This publication may refer to information and protected by
copyrights or patents and does not convey any license under the patent rights of SFRI Sarl, nor the
rights of others. SFRI Sarl does not assume any liability arising out of any infringements of patents or
other rights of third parties.
Warning
For continued safe use of this equipment, it is necessary that the listed instructions are followed.
However, instructions listed in this manual in no way supersede established medical practices
concerning patient care.
· This equipment is intended for use only by medical professionals in health care institutions.
· To avoid electrical shock, you should not open any cover by yourself. Service must be carried
out by qualified personnel only.
· It is dangerous to expose electrical contact or applicant coupler to normal saline, other liquid
or conductive adhesive. Electrical contact and coupler such as cable connector, power supply
must be kept clean and dry. Once being polluted by liquid, they must be thoroughly dried. If
to further remove the pollution, please contact your biomedical department or SFRI Sarl.
It is important for the hospital or organization that employs this equipment to carry out a reasonable
maintenance schedule. Neglect of this may result in machine breakdown or injury of human health.
Upon request, SFRI Sarl may provide, with compensation, necessary circuit diagrams, calibration
illustration list and other information to help qualified technician to maintain and repair some parts,
which SFRI Sarl may define as user serviceable.
Exemptions
SFRI Sarl's obligation or liability under this warranty does not include any transportation or other
charges or liability for direct, indirect or consequential damages or delay resulting from the improper
use or application of the product or the substitution upon it of parts or accessories not approved by
SFRI Sarl or repaired by anyone other than a SFRI Sarl authorized representative.
This warranty shall not extend to any instrument which has been subjected to misuse, negligence or
accident; any instrument from which SFRI Sarl's original serial number tag or product identification
markings have been altered or removed, or any product of any other manufacturer.
Warning
The H18 Light is an In Vitro Diagnostic instrument. It may indirectly bring risks to patients and present
a direct risk to operators and the environment during manipulation. To avoid these risks, be sure to
read the following instructions carefully.
This device uses AC 220V alternating courant. Do not open the rear cover before switching
off the power supply. If you need to open the rear cover of the device for maintenance
reasons, please contact our service personnel or professionals.
Patient samples are potentially contaminating agents. Manipulate with care using
appropriate protection equipment (glasses, gloves and laboratory coat) and be sure to
dispose of the waste in accordance with relevant regulations of your hospital.
Do not operate the device unless you have read this Operation Manual carefully
This Service Manual, in addition to the training courses run by SFRI Sarl FRANCE, is the basis for the
maintenance and repair of your 3 Part Diff Cell Counter H18 Light Version 2 (H18 Light V2, is H18 Light
with serial number above 02010411). This manual is intended only for suitably qualified service
technicians.
In the interest of the safety of patients and all operators:
Only service technicians trained and authorized by SFRI Sarl FRANCE may service the H18 Light V2.
Please refer to the operating instructions for any information you need on operating the H18 Light V2.
This Service Manual contains references to the corresponding chapters in the operating instructions.
(If required).
Class
According to anti-electric shock: Grade II, Pollution 2
According to defend deleterious liquid: General Equipment (Closed Equipment)
According to disinfection method: Recommend by manufactory
According to safety degree: Do not use the equipment under the environment of mixed with
flammable air or the air is mixed with O2 and NO
According to working state: Continuous running Equipment
Règlementation
DIV 98/79
Screen
Right Panel
Instrument
Status LED
Sample Probe
Window
Start Key
Thermal Printer
Door
Picture 1-1
11
1
12
2
13
3 14
4 15
16
5
17
6
18
19
8
9
10
Picture 1-2
# Description
1 Parallel Printer Port
2 PS2 Mouse Port
3 PS2 Keyboard Port
4 Equipotential Connector
5 Power Switch
6 Lyse Inlet Tube Connector
7 Waste Full Sensor Connector
8 Waste Outlet
9 Cleaner Inlet Tube Connector
10 Diluent Inlet Tube Connector
11 Cooling Fan (Expulses air)
12 USB Port 1
13 USB Port 2
Table 1-1
Measured parameters
ITEMS UNITS
9
WBC 10 / L
RBC 1012 / L
MCV fL
HGB G/L
PLT 109 / L
MPV fL
Table 1-2
Parameters given by histogram
ITEMS UNITS
LYM% %
MON% %
GRAN% %
RDW-SD fL
RDW-CV %
PDW %
P-LCR %
Table 1-3
Calculated parameters
ITEMS UNITS
LYM# 109 / L
MON# 109 / L
GRAN# 109 / L
HCT %
MCH pg
MCHC g/L
PCT %
Table 1-4
1.3.3. DILUTION
Dilution Ratio
Venous and Capillary mode: Prediluted Mode:
WBC/HGB 1:300 WBC/HGB 1:355
RBC/PLT 1:44600 RBC/PLT 1:44500
Display Language
8” LCD screen English
High resolution: 640x480 mm
Color display
1.3.4. INPUT/OUTPUT
1.3.5. PRINTOUT
H18 Light measures 330(W) x 430(H) x 380(D) mm. There should be adequate space for the
instrument as well as the mouse, keyboard, external printer (optional), external barcode
reader (optional). Make sure that there is at least 15 cm of clearance around the top, sides and
back of the instrument. Ensure that there is adequate space for reagents either under the
counter or at counter level. Instrument weight is 17,5 kg. Make sure you will enough space to
perform annual preventive maintenance or on demand repair.
The H18 Light should be located in a controlled environment free from dust, mechanical
vibrations, loud noises and electrical / magnetic interferences. Avoid proximity to brush type
motors, flickering fluorescent lights and electrical contacts that regularly open and close. Avoid
placing the instrument in direct sunlight or in front of a source of heat or drafts. The instrument
should be kept in a temperature controlled environment between 18°C to 35°C (65°F to 95°F)
with humidity between 10% to 90% non-condensing.
H18 Light requires a properly grounded outlet supplying 100 – 264 Va.c., 47 to 63 Hz. Power
consumption is 150 VA max.
We recommend the use of a 300 VA UPS.
Humidity should be less than 70%
Atmospheric pressure has to be between 86.0 and 106 kPa.
NOTE: theft or damage to the H18 Light and related systems is not responsibility of SFRI France. It is
responsibility of the consignee to fill all claims with the freight carrier and to make sure that all
shipments are properly insured.
Picture 2-1
viii. Take out the tie wrap blocking the sample arm like shown in the photograph bellow
Picture 2-2
Picture 2-3
Picture 2-4
x. Remove the fluidic ports protectors in the back side of the unit
xi. Connect the reagents supply tubes in the inlet fluidic ports (rear panel).
xiv. Connect the waste tube assembly to the back of the H18 Light.
We call background a measurement done without aspirating any blood, but air. In order to
avoid registering the results of background tests in the DATALOG, you may enter 999999 code
in patient Id.
Press the Start Key without presenting any tube to the sample probe and let the instrument
perform a complete counting cycle. The results given by the unit should comply with the
following table:
Item Range
WBC 0.0 – 0.2 x 109/L
RBC 0.00 – 0.02 x 106/µL
PLT 0 – 6 x 103/µL
HCT 0.0 – 0.5 %
Table 2-1
Should the Background results be out of tolerances, please refer to Trouble shooting section.
2.4.2. STABILITY : CV
Once the system is able to perform at least five backgrounds in range you can go through the
stability verification.
Run 15 replicates of a normal level SFRI blood control in factory mode (Refer to Software
Chapter) and make the instrument calculate for you the CV.
If the CV values are in range (see table 2-2 below), then see if they are in target, ie, if the results
comply with the control target. If they match, the system is ready to be used. If they are not
you have to perform a calibration.
IMPORTANT NOTE:
H18 Light System has two sets of calibration factors.
One set is the factory one, and can be seen and adjusted in “Factory” mode of the software.
The second set is the user one, and can be adjusted manually or automatically by the user, in
“Normal” software mode.
If your system is stable and the values are not in range, you may need to calibrate the unit.
Use only SFRI Calibration Blood, and follow the calibration procedure as described in Operator
Manual version H18 LIGHT_Operator Manual_ENG_V12.00 or above.
The Coulter principle states that particles pulled through an orifice, concurrent with an electric
current, produce a change in impedance that is proportional to the volume of the particle
traversing the orifice. This pulse in impedance originates from the displacement of electrolyte
caused by the particle. The Coulter principle was named for its inventor, Wallace H. Coulter
when he was working for the Department of Naval Research to standardize the size of solid
particles in the paint used on US battleships in order to improve its adherence to the hull. The
principle has found commercial success in the medical industry, in particular in hematology,
where it can be applied to count and size the various cells that make up whole blood.
Cells, being non-conducting particles, alter the effective cross-section of the conductive micro
channel. If these particles are non-conducting, the electrical resistance across the channel
increases, causing the electric current passing across the channel to briefly decrease. By
monitoring such pulses in electric current, the number of particles for a given volume of fluid
can be counted. The size of the electric current change is related to the size of the particle,
enabling a particle size distribution to be measured, which can be correlated to mobility,
surface charge, and concentration of the particles.
Picture 3-1
The Coulter principal basically deals with the well known Ohm low:
U=RxI
U = f(ps)
3.1.2.1. THREASHOLDS
Each cell crossing the apertures will create a signal, a voltage pulse, which amplitude will
be compared to triggers, allowing their classification on WBC, RBC and PLT. These
thresholds are software values that are inside the executable program. Neither the user
nor the service people are able and allowed to modify these values.
3.1.2.2. HISTOGRAMS
Each pulse will be analyzed and stored to a specific memory area, depending on its
characteristics. Once the counting time is over (after 12 seconds), the memorized data is
processed and the histograms are performed. It is then possible to get any histogram
derived data.
Picture 3-2
After initialization and between each sample counting, the unit is in standby mode.
All the reagents are primed and the chambers are filled with diluent.
Vacuum / Pressure chamber is at atmospheric pressure.
The constant current generator is off.
Burn voltage is off.
Dilution mechanism and vacuum /pressure mechanism are at home position while sample
probe arm is positioned ready to pipette a new sample blood.
All valves are off (ie, not energized). Two ways valves are closed, and three ways valves are in
NO (Normally Opened) position.
HGB lamp is on.
Motors power is off.
4.1.2. DILUTION
The blood tube is presented to the sample probe, start switch is pushed, 14 µL of sample is
aspirated. A first dilution is done in the WBC chamber. Dilution ratio is 1/300 in venous and
capillary mode. A little amount of volume is then aspirated to prepare the second dilution in
the RBC chamber. Dilution ratio is 1/44600. Lyse is dispensed to WBC chamber: 500 µL. HGB is
read by the spectrophotometer.
4.1.3. COUNTING
As soon as the dilutions are ready in both chambers, the vacuum/pressure pump generates an
accurate and stable counting vacuum. The cells are then hydro-focused in a fluidic current in
order to be counted separately during 12 seconds.
Simultaneously, RBC, PLT, and WBC are counted. RBCs and PLTs are counted in the RBC
chamber and the WBCs are counted in the WBC chamber.
The software is controlling the consistency of cells circulation in order to detect any fluidics
problem.
4.1.4. CLEANING
Picture 4-1
Picture 4-2
The second dilution is performed in this chamber used to count the RBCs and the PLTs. Its ratio
is 1/44600.
The aperture of this chamber has an 80 µm orifice and the aperture voltage range is between
13 Vdc and 23 Vdc. The ruby separates two areas of the chamber; in each of them an electrode
is located, driving either the counting controlled constant current or the “high AC voltage”, in
charge of the burning function coming from the CCU board.
The electrodes of the chamber are connected to the CCU Board at J28 / J30
The HGB Assy is mounted on this chamber: LED 540 nm light source, and photo sensor. Both
are connected to CCU board to connector J21.
FUNCTIONS:
The function of this assembly is to prime and aspirate / dispense reagents, sample blood
(sample, control, and calibrator). It is composed of a single Teflon block, in which 3 chambers
and their corresponding pistons are in charge to deliver accurate volumes of blood, diluent
and lyse.
The three pistons are mechanically linked and thus are moving at the same time. The valves
activation program allows proper volumes delivery as required.
IMPORTANT: the sample piston has a specific design, making possible to control the other two
pistons without any consequence on the sample one. Two mechanical stops, located at specific
position allow this to be possible. Refer to picture 4-8 below (mark 2).
Picture 4-8
FUNCTIONS :
ü Counting vacuum: provide: accurate and stable vacuum for the counting phase
ü Mixing: Provide positive pressure to send air bubbles to the chambers, mixing function
ü Priming the cleaner during cleaning phase
ü Waste the vacuum pump contain
Picture 4-9
FUNCTIONS:
Wash the external part of the sample probe after blood aspiration
Picture 4-10
ITEM CODE: S020007 (Two way valve) / ITEM CODE: S020008 (Three way valve)
FUNCTION TABLE
5.1.2. FUNCTIONS
- Provide +12Vdc and +5Vdc to CPU board (via CCU, and jumper JP1) and CCU board
- +5Vdc / 4A is intended to power the CPU board
- +12 Vdc is intended to power the CCU board
- Provide +5Vdc and +12Vdc to
-
5.1.3. NOTE
- An internal trimmer allows the adjustment of these voltages, paying attention that the
CPU voltage mustn’t be lower than 4,5 Vdc
- Two fuses of 3,15A (delayed)
5.2.2. FUNCTIONS
5.2.2.1. ACTUATORS
o Motors driver
§ Motor A (1): Sample probe vertical movement
§ Motor B (2): Sample probe horizontal movement
§ Motor C (3): Dilution block movement
§ Motor D (4): Vacuum / Pressure pump
o 2 ways valves
o 3 ways valves
o Constant current generator (coulter principal cells counting)
o High AC voltage for “burn” function
5.2.2.2. SENSORS
The board has been developped around a CPLD (Complex Programmable Logic Device)
powered by a voltage of 3,3 Vdc, supplied by the positive voltage regulator LT1117.
Picture 5-1
Picture 5-2
Picture 5-3
Connector # Description
J1 Not Used
J2 Power Supply
J3 Home Sensor Motor A (Probe Vertical Movement)
J4 Command Power Motor A
J5 Home Sensor Motor B (Probe Horizontal Movement)
J6 Command Power Motor B
J7 PC 104 Connector
J8 Home Sensor Motor C (Dilution Block)
J9 Command Power Motor C
J10 PC104 Connector
J11 Home Sensor Motor D (Vacuum Pump)
J12 Command Power Motor D
J13 Solenoid Valves Connector (V1 to V8)
J14 Solenoid Valves Connector (V9 to V14)
J15 Lyse presence detector (optical sensor)
J16 Distribution Board
J17 Cleaner presence detector (optical sensor)
J18 Diluent presence detector (optical sensor)
J19 Waste Full Sensor (Resistive)
J20 Start Switch
J21 HGB Sensor Assy
J23 Diluent Temperature
J24 On Board Thermal Printer
J25 WBC Chamber
J26 Front Panel LED Status Indicator
J27 Burn Trasnformer
J28 RBC Chamber
Table 5-1
TP # TP Description Comment
TP1 Ground
TP2 Not Used
TP3 2,5 Vdc
TP4 Reagent Temperature Sensor
TP5 Cleaner Presence Sensor Typical value 4 Vdc with liquid, bellow 1,5 Vdc without
TP6 Not Used Not Used
TP7 Diluent Presence Sensor Typical value 4 Vdc with liquid, bellow 1,5 Vdc without
TP8 Lyse Presence Sensor Typical value 4 Vdc with liquid, bellow 1,5 Vdc without
TP9 RBC Counting Pulses
TP10 Not Used Not Used
TP11 PLT Counting Pulses
TP12 A/D Convertor Clock
TP13 WBC Counting Pulses
TP14 HGB OD Signal
Table 5-2
5.3.2. FUNCTIONS:
This is the HID of the instrument. This industrial computer provides all basic input and output
system for the user, and communication with machine level software, ie, communication with
the CCU firmware through a PC104 bus.
A compact flash memory, or a Disc On Module, connected to the CPU, contains all BIOS, OS
and application software, allowing the unit to operate. The picture below shows all the
connectors detail.
Picture 5-4
5.4.2. FUNCTIONS:
This board interfaces the connections between the CCU board and the actuators and sensors.
It also has a dedicated electronics to adjust the optical reagent detection sensitivity, as shown
in detail E.
Detail D shows the valves connection interface, detail C the sensors, and detail B the actuators.
Picture 5-6
5.5.2. FUNCTION:
The main function of LCD Adaptor Board is to connect the screen to the CPU with cable. It
interfaces TFT through FPC soft cable.
Picture 5-7
Picture 5-8
Picture 6-1
6.1.2. FUNCTION
This mechanical assembly allows the system to position the sample probe at operator disposal,
to aspirate the sample, calibrator or control blood and then to the counting chambers, in order
to perform the dilutions.
While performing maintenance, the mechanical system will cover the same function but
Hemaclair or Diluclair will replace the blood.
Two movements are carried out to perform these positioning: vertical and horizontal.
Thus, two stepper motors are involved, Motor A (vertical movement), and Motor B (horizontal
movement). Each movement has a home position, controlled by an optical sensor.
Picture 6-2
Picture -6-3
7.1. Mechanics
This Service Program allows the service engineer to troubleshoot, by checking actuators and sensors.
Basically, this program sends single commands to the CCU.
Picture 7-1
Picture 7-2
NOTE: Valves 1, 7 and 8 are not used. The “T” command is grey, and a click on it has no effect.
Valve 15 actually is a relay command
7.1.2. MOTOR
A click on “T” command of each motor will generate a movement to get the mechanical part
to home position. If the mechanism is already at home position the firmware will move the
flag out and in again. If the mechanism is out of home position the firmware will move the flag
toward home position.
If the system doesn’t detect any error on the movement the software will send an “Ok” status,
otherwise “Failed” will be prompted.
ü Motor A: Vertical Movement of the Sample Probe Arm
ü Motor B: Horizontal Movement of the Sample Probe Arm
ü Motor C: Dilution Block Movement
ü Motor D: Vacuum Pump Movement
7.1.3.3. 5V POWER
This is an integrated voltmeter returning the actual +5 Vdc value.
7.1.3.4. HGB
This function returns the actual HGB sensor reading. Please refer to Adjustments and
Controls chapter for more details.
7.1.3.5. VACUUM
This function creates a specific vacuum value (counting vacuum). Activating this command
will make the vacuum piston move up to predefined specific position.
7.1.3.6. DC POWER
This is the “Enable” signal sent by the software to the CCU board.
7.1.3.7. CC POWER
This function allows you to test the Constant Current generator. A click on its “T” command
will activate relays K4 and K5, as a result the Constant Current will be sent to the electrodes
of both counting chambers inorder to generate the base line voltage.
7.1.3.8. BURN
This function sends 110 Vac directly to the electrodes of both counting chambers in order
to clean the apertures and prevent clogs that could appear due to orifice diameter
reduction while proteins get agglutinated. Relay K2 is activated to send this “high” AC
voltage to the chambers.
7.1.3.9. R. TEMP
This function returns the actual diluents’ temperature, measured by the sensor integrated
in the sample line.
7.1.3.10. SPEAKER
Internal speaker test. You should hear a little “pock” sound.
Then the system goes back to stand by, ie, stops the constant current and the diluent
circulation. The measured value remains in the screen.
An action on the T2 command will refresh the actual baseline voltage value that has to drop
below 3 Vdc. Tipical value is around 1,5 Vdc.
7.1.3.12. INTERFACE
You can test the three peripheral dedicate to receive results.
ü On board thermal printer (Recorder)
ü External Printer
ü RS232 Serial Port
7.2. Special
7.2.1. FACTORY MODE
IMPORTANT NOTE: never leave the unit with factory mode accessible
for the end user.
All the standard functions of the unit are the same than in user mode.
You should print and save these parameters before sending the unit at customer site
7.2.2.1. PARA
Do not attempt to adjust these parameters, they are factory set and don’t need any
adjustment in the field, unless SFRI authorized specialist indicates you to perform changes
there.
7.2.2.2. FLUIDICS
WBC & RBC Time (s): Software fixed at 12 seconds. This value mustn’t be changed.
WBC & RBC Hole: These are the reference values that the system uses in order to return a
clog situation. Refer to adjustment chapter for procedure.
WBC & RBC threshold: Factory values that don’t have to be changed.
Temp. Low: sets the minimum room temperature allowed to the system to work.
Temp High: sets the maximum room temperature allowed to the system to work.
Motor A, B, C and D: motor steps for mechanics positioning. Factory adjusted, they don’t
have to be modified.
SFRI H18 Light hematology analyzer use RS-232 port as a network transmission. There are
three data lines on transmission: TxD, RxD, GND. The data transfer to the receiving device by
an one-way transmission, not response of data request for any external device. This protocol
adopts characteristic identification method and data block on transmission. All the decimal
points could not be transferred in practice.
Table 7-1
7.3.3. WIRING
Picture 7-4
The total number of the received data between (0,255) is 256. If there are 256 points on the
X-axis of the histogram, set the proportion of Y-coordinates as “a”. Divide the 256 received
data respectively by “a”, the results as the values of Y-coordinates. Draw the corresponding X-
coordinates in the received order.
7.3.6. EXAMPLE
@a05060300820050603214308069#269#121#610#019#008#042#420#095#361#0860#0226#0263#
465#150#117#097#113#011#141####################################0200570822550101640
10214########00000000000000000000000000000000000000000000000000000000100200200300
Use Hyper Terminal or HTerm and a female / female DB9 crossed RS232 cable, using only RxD, TxD
and GND.
The related data of the transfer is shown in the following result printout
Picture 7-5
After each Preventive Maintenance, or as required during troubleshooting, error or warning messages,
some controls and / or adjustments may be performed. You will read bellow the detailed explanation
/ procedure for each adjustment and control.
Picture 8-1
Picture 8-2
At this time, it should issue a crisp Di Di sound, Waste Full alarm will be displayed in the right bottom
area of the screen.
When the system runs out of reagent, Diluent Empty, Lyse Empty and Cleaner Empty alarm
information will be displayed in the error message area of the screen.
Unplug the waste liquid short circuit connector on the back board of the H18 Light, power off and on.
The instrument should be able to start, without any warning message.
Clicking on T button makes the corresponding valve commutate, remaining open for a couple of
seconds. You must hear the mechanical sound of commutation, taking in account that two way valves
have a louder sound than the 3 way valves.
8.4.2. INT
The Interruption Controller is responsible for the cells signals acquisition. To check the
interruptions request click T command of each channel, each microcontroller. The status
screen will return OK or FAILED.
Picture 8-3
Picture 8-3
iii. In the same fitting of the vacuum pump, connect the vacuum meter tubing, as shown I
photograph #2
Picture 8-4
vi. Click again on T button of Vacuum function. The piston will go down to home position.
vii. Disconnect the manometer tubing, and put in place the original tubing.
ü Open the right panel of the unit by unscrewing the two allen screws (2.5 mm), you can access
to the fluidics panel
ü Set voltmeter to Vac
ü Introduce the red probe of the voltmeter inside the WBC/RBC chamber and apply the black
probe to ground, as shown on the photograph below:
ü Click on T button of Burning function
ü You should read a value around 90 Vac (the relay remains switched a very short time, so the
reading of the target value is furtive).
Clicking T2 command will switch off the constant current to the electrodes. At that moment the
residual voltage displayed have to be less than 3 Vdc for both chambers.
Click “Service”—“Special”, in the pop-up message box input password: “6666”, click OK, press
F12 on the keyboard, to make the host enter into “Factory” mode “the system interface above
should display “factory”
Record the W.H.V.S. and R.H.V.S. after each test, calculate the average of 5 times W.H.V.S. and
R.H.V.S., and input into the Parameters (click Service----Special, in the pop-up message box
input WBC Hole and RBC Hole under password 6161)
Picture 8-6
ü Ask the user to perform a background before starting the working day. Check that the result is
in range.
ü Run a QC SFRI bloodtrol and check that the result is in target.
ü At the end of the day, perform a Shutdown using the Diluclair when the instrument prompts
you.
ü Clean the unit panels with neutral detergent. Clean the screen, keyboard and mouse as
requested with adequate cleaner.
For any brake down, malfunction, that the user is not able to handle, the end user
representative will have to contact the local SFRI representative technical service, in order to
proceed without delay to the relevant repair actions.
Table 9-1
Diluclair H18:
Name Diluclair H18
Presentation 60ml
code HSC301
exp 1 year from date of manufacture
Description Diluclair H18 is a concentrated enzymatic cleaner that
will increase efficiency of the cleaning. The proteolytic enzyme contained
will eliminate all traces of blood in the fluidic.
Benefit Regular use will significantly decrease the risk of
clogging and of incorrect backgrounds.
Risk This will increase the consumption of reagents and it
will provoke a waste of time due to more frequent cleanings of the
instrument and especially the fluidic.
The main operations that have to be performed during preventive maintenance (normally performed
in a three hours), are summarized in the PM (Preventive Maintenance) check list bellow.
Hemaclair / Diluclair
9.2.1.2. PROCEDURE
Replace seals and cleaning
Vacuum Pump
The seal of the vacuum pump piston must be replaced after one year (or after 6 months if number of
samples / day > 30), to ensure proper functioning (stable and accurate vacuum counting value).
1/ Disassemble the bearings bracket, by unscrewing the 3 screws, which allow you to take out easily
the rod and the piston from the block (1, 2 and 3).
1 2 3
Picture 9-3
2/ Take out the tubes from the vacuum pump, push up gently the rod and the piston to take them out
from the block.
4/ Clean the vacuum pump piston with an ultrasonic washing device or distilled water.
Picture 9-6
7/ Take out the seal from the block and clean the vacuum pump with ultrasonic washing device or
distilled water.
8/ Replace the seal with a new one. Re-assemble the parts and respect the order of assembling.
2/ Take out gently the two pistons (Lyse piston and Diluten piston) from the block by pushing down
the metal part to create a space and the pistons for disassembling from the block.
3/ Unscrew the five screws to remove Teflon bracket covering seals and o-ring.
5/ Use the sample piston to turn the cable gland. “a quarter turn!”
6/ Take out the Diluents and Lyse seals from the block.
8/ Clean all the parts of the dilution block by using the cleaning ultrasonic device or any equivalent
cleaning equipment. Re-assemble the sample piston as shown.
Picture 9-22
1/ Unscrew the screw to disconnect the electrical grounding wire (black cable) from the chamber (not
forget to disconnect also from the CCU Board)
5/ Clean the ruby and the silicon spacers with the ultrasonic device or Hemaclair.
CAUTION: there is only one correct way to place the ruby. Please refer to draft bellow.
Picture 9-29
1/ Take out the tubes from the washing head (2 tubes) and unscrew the two screws on the top of the
washing head (2 screws)
2/ gently push down the washing head, to take it out from the sample probe.
Disassemble the top part from the block to take out the seal from the washing head.
This chapter gives instructions for identifying, troubleshooting, and correcting instrument problems. If
you cannot solve the problems according to this guidance or you wish to get more information, please
contact your local distributor.
Table 10-1
Picture A4-1
Picture A4-2
Picture A4-3
Picture A4-4
Picture A4-5
Picture A4-6
Picture A4-7
Picture A4-8
Picture A4-9
Picture A4-10
Picture A4-11
Picture A4-12
12th Step: Aspiration of Blood and Diluent (Mixed) from the WBC chamber.
Picture A4-13
Picture A4-14
Picture A4-15
Picture A4-16
16th Step: Empty the blood and diluent (Mixed) in RBC chamber and add lyse in WBC chamber.
Picture A4-17
Picture A4-18
Picture A4-19
Picture A4-20
Picture A4-21
Picture A4-22
Picture A4-23
Picture A4-24
Picture A4-25
Picture A4-26
Picture A4-27
Picture A4-28
END OF PROCEDURE