Professional Documents
Culture Documents
2. Troubleshooting .......................................................................................... 6 - 42
3. Procedures .................................................................................................. 7 - 42
1. Tools ............................................................................................................... 9 - 2
2. Kits ................................................................................................................. 9 - 3
3. Fuses .............................................................................................................. 9 - 3
4. Stickers .......................................................................................................... 9 - 4
8. Troubleshooting ........................................................................................ 10 - 27
3. Procedures .................................................................................................. 11 - 7
1. Document update
1.1. Revisions
This document applies to the latest software version listed and higher versions.
All information included in this document is current as of the date of creation of this version. Changes
that may occur will be available on ITS Web site http://its-information.horiba-abx.com/.
This manual applies to both ABX Pentra 400 and Pentra C400.
For the ABX Pentra 400, this manual is intended for use on instruments with serial numbers
above 2999 (V3).
In some procedures, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
■ V2 corresponds to instruments with serial numbers between 2000 and 2999.
2. Legal information
This product complies with the Standards and Directives named in the Declaration of Conformity.
The latest version of the EC Declaration of Conformity for this product is available on www.horiba-
abx.com/documentation.
The information in this manual is distributed on an "As Is" basis, without warranty. While every
precaution has been taken in the preparation of this manual, HORIBA Medical will not assume any
liability to any persons or entities with respect to loss or damage, caused or alleged to be caused directly
or indirectly by not following the instructions contained in this manual, or by using the computer software
and hardware products described herein in a manner inconsistent with our product labelling.
2.3. Trademarks
2.4. Graphics
All graphics including screens, printouts and photographs are for illustration purposes only and are not
contractual.
To alert the operator of potentially hazardous conditions, symbols described in this chapter are provided
wherever necessary throughout the manual.
Emphasizes information that must be followed to avoid hazard to either the operator or the
environment, or both.
Emphasizes information that must be followed to avoid possible damage to the instrument
or erroneous test results.
Emphasizes information that can be helpful to the operator before, during or after a specific
operational function.
All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any
means, electronic, mechanical, photocopying, recording, or otherwise, without the prior written
permission of HORIBA Medical.
3. Operational conditions
3.1. Environment
The operation of the ABX Pentra 400 / Pentra C400 should be restricted to indoor location use only.
The instrument is operational at an altitude of maximum 3000 m (9840 ft).
The instrument is designed for safety from voltage surges according to INSTALLATION CATEGORY II
and POLLUTION DEGREE 2 (IEC 61010-1).
3.2. Location
Keep in mind that the instrument weighs approximately 120 kg (265 lb).
To move the instrument, four persons are required.
The lifting handles provided in the installation kit must be used.
The Power switch and Power supply connection should always be accessible. When
positioning the system for operational use, leave the required amount of space for easy
access to these items.
3.3. Grounding
Proper grounding is required when installing the system. Check the wall outlet ground (earth) for proper
grounding to the facilities electrical ground. If you are unsure of the outlet grounding, contact your
facilities engineer to verify the proper outlet ground.
■ Instrument operating temperature: from +15°C (+59°F) to +32°C (+90°F). If the instrument is stored
at a temperature lower than 10°C (50°F), it should stand for one hour at normal room temperature
before use.
■ Humidity Conditions: Relative humidity of 20% - 85% maximum, without condensation.
■ Temperature gradient: 2°C (3.6°F) per hour.
The instrument has been designed to produce less than the accepted level of electromagnetic
interference in order to operate in conformity with its destination, allowing the correct operation of other
instruments also in conformity with their destination.
In case of suspected electromagnetic noise, make sure that the instrument has not been placed in the
proximity of electromagnetic fields or short wave emissions, e.g. Radar, X-rays, Scanners, Cell phones,
etc.
Do not perform analysis while cover is open or not correctly fixed. Electromagnetic noise can
affect the data or disrupt a nearby instrument.
Grounding is required. Make sure the earth wall-plug is correctly connected to the laboratory grounding
system. If there is no such system, a ground stake should be used.
Use only the main supply cable delivered with the instrument.
Main power supply voltage fluctuations must not exceed +/- 10% of the nominal voltage.
Instrument disposal
This product should be disposed of and recycled at the end of the useful life in accordance
with European Directive 2002/96/EC on Waste Electrical and Electronic Equipment (WEEE)
and/or European Directive 2006/66/EC on batteries and accumulators.
Instrument storage and transportation temperatures: from -20°C (-4°F) to +50°C (+122°F).
Analyzer exposure to rainfall and extended sunlight must be avoided. The outdoors storage of the
analyzer is prohibited.
Keep in mind that the instrument weighs approximately 120 kg (265 lb).
To move the instrument, four persons are required.
The lifting handles provided in the installation kit must be used.
Before instrument removal from use, transportation or disposal, perform a general cleaning and a
draining of your instrument.
3.9. Package
Factory package of the analyzer ABX Pentra 400 / Pentra C400 and its implements consists of firm
corrugated cardboard, polyethylene foil and inner foam plastic framework. Package protects analyzer
and its implements from adverse factors of outside environment.
Analyzer must be transported in its original factory package.
1. Technical specifications............................................................................... 2 - 2
1.1. Intended use .............................................................................................................................. 2-2
1.2. Analysis methods....................................................................................................................... 2-2
1.3. Throughput ................................................................................................................................ 2-2
1.4. Reagent...................................................................................................................................... 2-2
1.5. Sample....................................................................................................................................... 2-3
1.6. Calibrator and control ................................................................................................................ 2-4
1.7. Computer characteristics .......................................................................................................... 2-4
1.8. Measurement ............................................................................................................................. 2-4
1. Technical specifications
The ABX Pentra 400 / Pentra C400 system is a fully automated chemistry analyzer using colorimetry,
turbidimetry and potentiometry technologies. It is mostly meant to be used for in vitro diagnostic
analyses based on homogeneous samples such as serum, plasma, urine and whole blood.
The ABX Pentra 400 / Pentra C400 system allows analysis by:
■ Colorimetry
■ Turbidimetry
■ Potentiometry: direct for serum and plasma, indirect for urine (ISE module option)
1.3. Throughput
1.4. Reagent
Packaging accepted
■ Twin compartment cassette 30/10 from HORIBA Medical
■ Twin compartment cassette 50/50 from HORIBA Medical
■ Twin compartment cassette 70/30 from HORIBA Medical
■ Twin compartment cassette 80/10 from HORIBA Medical
■ Single compartment cassette 100 from HORIBA Medical
■ Reagent rack
On board conditions
■ Capacity: 52 cassettes (39 tests with reagent racks)
■ Temperature: 44 positions refrigerated at 4°C - 10°C (39°F - 50°F) and eight positions at room
temperature
Reagent management
■ Barcode reagent identification
■ Back-up for same reagent
■ Remaining volume calculation
■ Automated reagent on board stability check
Reagent sampling
■ Volume:
- Minimum: 2 µL with sample needle and 15 µL with reagent needle
- Maximum: 600 µL
■ Capacitive level detection
■ Insufficient volume detection
■ Reagent preheating at 37°C +/- 0.5°C (98.6°F +/- 0.9°F)
1.5. Sample
Sample types
■ Serum
■ Plasma
■ Urine
On board conditions
■ Capacity: 60 samples
■ Continuous loading
Sample management
■ Barcode sample identification:
Barcodes from two to 16 digits.
Accepted barcode types:
- ITF 2/5 (2 of 5 interleaved) with or without check digit
- Code 39 with or without check digit
- Code 128
- Codabar
■ Tube presence detector
Sampling
■ Volume:
- Minimum: 2 µL
- Maximum: 95 µL for one step and 380 µL for four steps
■ Automatic sample dilution: 1/2 to 1/22500
■ Automatic post-concentration: x2 to x10
■ Capacitive level detection
■ Shock detection
■ Clot detection and insufficient volume detection
Calibrator/Control positioning
Sample tray and reagent tray
1.8. Measurement
Reaction system
■ Reaction cuvettes: disposable acrylic cuvettes
■ Cuvette volume: 150 µL - 600 µL
■ Automatic loading and unloading of cuvettes
■ "New cuvette" holder capacity: 360 cuvettes
■ "Used cuvette" holder capacity: 360 cuvettes
■ Mixing: stirring paddle
■ Reaction temperature: 37°C +/- 0.2°C (99°F +/- 0.36°F), air bath controlled
■ Measurement cycle: 12 seconds
■ Sampling cycle: 12 seconds
■ Reaction time: 12 seconds - 20 minutes
Optical system
■ Measurement principle: absorbance measurement (Bichromatic or Monochromatic)
■ Light source: tungsten-halogen lamp
■ Diffraction: concave reflective grating spectrograph
■ Detector: photodiode array
■ Wavelengths: 340, 380, 405, 420, 455, 490, 505, 520, 550, 560, 580, 600, 620, 660, 700 nm
■ Optical linearity:
Algorithms supported
■ Factor
■ Slope average
■ Linear regression
■ Linear interpolation
■ LOGIT/LOG4
■ LOGIT/LOG5
■ Exponential
2. Physical specifications
■ Power supply:
- Instrument: from 100 V to 240 V (+/- 10%), 50 Hz to 60 Hz
- Cooling unit CU401 (depends on models):
100 V (+/- 10%), 50 Hz to 60 Hz
115 V (+/- 10%), 60 Hz
230 V (+/- 10%), 50 Hz
230 V (+/- 10%), 60 Hz
- Cooling unit CU400 (depends on models):
100 V (+/- 10%), 50 Hz to 60 Hz
115 V (+/- 10%), 60 Hz
230 V (+/- 10%), 50 Hz to 60 Hz
240 V (+/- 10%), 50 Hz
■ Maximum power consumption:
- Instrument: 250 VA
- Cooling unit CU401: 700 W
- Cooling unit CU400: 450 W
■ Maximum heat output:
- Instrument + cooling unit CU401: 1940 BTU/h (2010 kJ/h)
- Instrument + cooling unit CU400: 2080 BTU/h (2160 kJ/h)
■ Printer: refer to your printer manual.
Fuses characteristics:
Slow-blow internal fuses having the following characteristics: 2 x T 6.3 A H 250 V (5x20 mm)
■ De-ionized/distilled water
■ Water specifications:
- Resistivity > 5 Mohm.cm
- Conductivity < 0.2 µS/cm
3. Temperature control................................................................................... 3 - 12
3.1. PID control ............................................................................................................................... 3 - 12
3.2. Reagent tray ............................................................................................................................ 3 - 15
3.3. Reagent needle........................................................................................................................ 3 - 20
3.4. Reaction tray............................................................................................................................ 3 - 21
5. Pressure detection...................................................................................... 3 - 28
5.1. General points.......................................................................................................................... 3 - 28
5.2. High pressure, low pressure and bad sampling detection ...................................................... 3 - 29
1. Optical principles
The biochemistry analysis principle is to mix some reagents with a sample to produce a chemical
reaction. The reactive solution thus produced presents absorption properties at a specific wavelength.
The absorbance measures the reactive solution capacity to absorb the light that travels through it, at a
specific wavelength.
The absorbance is defined as follows:
A = log (I0 / I)
A Absorbance
I0 Intensity of light before it travels through the reactive solution
I Intensity of light that has passed through the reactive solution
Cuvette with
reactive solution
l = 0.6 cm
The Beer-Lambert law states that the measured absorbance at a specific wavelength is
proportional to the length of solution that the light travels through, and also the concentration of
the absorbing substance in the solution.
A=ε*l*c
A Absorbance
ε Absorption coefficient of the absorbing substance at a specific wavelength
l Length of solution that the light travels through
c Concentration of the absorbing substance in the solution
In the ABX Pentra 400 / Pentra C400 case, the length of solution that the light travels through is fixed
(l = 0.6 cm) as the absorption coefficient of the absorbing substance at a specific wavelength. So, the
measured absorbance at a specific wavelength is proportional to the concentration of the absorbing
substance in the solution.
In conclusion, the concentration of the absorbing substance in the solution is a function of the intensity
of light that has passed through the reactive solution, at a specific wavelength.
c = [ 1 / (ε * l) ] * log (I0 / I)
■ White light from the halogen tungsten lamp is collected by the condensing lens.
■ Once reflected by the folding mirror and shaped by the second lens, the white light beam passes
through the cuvette where it travels through the reactive solution.
■ White light emerging from the cuvette is then coupled with the spectrograph entrance slit by the third
lens.
■ The concave reflective grating spreads the incoming white light into monochromatic radiations and
reflects them onto the photodiode array.
white light
monochromatic radiations Concave reflective grating
■ For the ABX Pentra 400 / Pentra C400, the monochromatic radiations of diffraction order +1 are used
and reflected onto the photodiode array.
■ The concave reflective grating focuses all the wavelengths onto the photodiode array.
■ For the ABX Pentra 400 / Pentra C400, the photodiode array measures the light intensity for 15
wavelengths: 340, 380, 405, 420, 455, 490, 505, 520, 550, 560, 580, 600, 620, 660, 700 nm.
During a complete spectrophotometer initialization, the steps 1 to 6 (described below) are performed.
The gains, expressed in % in the Spectro menu (Services > Diagnostics > Spectro), correspond to the
amplification percentages applied for each wavelength (from 0 to 100%). These amplification
percentages are directly proportional to the multiplier coefficients applied for each wavelength.
The gains should be included between 1 and 95%.
■ If one of the gains is > 95% and ≤ 98%, the lamp is still operational but dying and a warning is triggered
(#629 "The lamp is dying, it is still operational but you will need to change it soon.").
■ If one of the gains is < 1% or > 98%, the lamp needs to be replaced at once and an alarm is triggered
(#520 "The lamp has failed the gain check. Please change the lamp.").
1 95 98
Lamp Detector
Inter-sector
Lamp Detector
IB must be included between 1400 and 2000 for all the wavelengths.
No warning or alarm is triggered if IB is out of these ranges.
Empty cuvette
Lamp Detector
A Absorbance
IA Light intensity on air
IB Black intensity
IC Light intensity on empty cuvette
The absorbance at 340 and 700 nm is checked to ensure that it is included in the cuvette presence range
as in the cuvette cleanness range.
Water-filled
cuvette
Lamp Detector
The steps 1 to 6 (described above) are automatically performed every time the instrument is:
■ turned on
■ woken up after a "stand-by"
■ initialized after a lamp replacement from the Customer Services menu (Services >
Customer Services > Cycles) or a modification of spectrophotometer gain adjustment
from the Spectro menu (Services > Diagnostics > Spectro).
Cuvette Exit
Start up or Lamp Measure
Steps Routine segment "Diagnostics"
wake up replacement gain
replacement menu
Gain adjustment
X X X
and check
Light stability check X X X
Light intensity on air
X X X X
(IA)
Black intensity (IB) X X X
Cuvette cleanness
X X X X X X
check (IC)
Reference light
X X X
intensity (IW)
Cuvette with
reactive solution
Lamp Detector
A Absorbance
IW Reference light intensity on water-filled cuvette
IB Black intensity
I Transmitted light intensity
8. Bichromatism principle
The ABX Pentra 400 / Pentra C400 measures the absorbance at two different wavelengths to correct the
absorbance due to a cuvette defect, some sample interferences, etc.
The primary wavelength is used to measure the reactive solution absorbance.
The secondary wavelength is used to measure the absorbance due to a cuvette defect, some sample
interferences, etc.
The absorbance is corrected as follows:
A = A1 - A2
A Absorbance
A1 Measured absorbance at the primary wavelength
A2 Measured absorbance at the secondary wavelength
2. Fluidic principles
Sales
Mark on diagram P/n Designation
unit
EBA010A
LV1, LV2, LV3 VALVE, 2 WAYS ELECTROVALVE 1
(1202351010)
EBA011A
LV4, LV5 VALVE, 3 WAYS ELECTROVALVE 1
(1202351011)
NEEDLE MANIFOLD
1300015267 MANIFOLD, WITH VALVES V1 AND V2 1
(LV1-LV2)
XCA194B
MANIFOLD (LV3-LV5) VALVE, 3 VALVES ASSY 1
(1209122194)
9001072
FILTER FILTER, FILTER LIQUID COMPLETE 1
(1229001072)
XEC202AS
B1 PUMP, WATER ASSY + METAL SHEET 1
(1209179202)
XCA216BS
B2 PUMP, WASTE ASSY + METAL SHEET 1
(1209129216)
XCA198B
LOW MANIFOLD FLUID, OVERFLOW MANIFOLD 1
(1209122198)
XCA197A
FLUID, CONDENSATION MANIFOLD V1 1
(1209121197)
EAB013A
E1 FITTING, STRAIGHT 3.1/2.3 CLEAR 1
(1202211013)
EAB015A Pack
E2 FITTING, STRAIGHT 2.5/1.5
(1202211015) of 5
0.89-xxx EAE004A* TUBING, TYGON 0.889 (0.035) *
2.06-xxx EAE008A* TUBING, TYGON 2.06 (0.081) *
2.29-xxx EAE009A* TUBING, TYGON 2.29 (0.090) *
C4x6-xxx EAE028A* TUBING, CRYSTAL 4X6 *
C4x7-xxx EAE043A* TUBING, CRYSTAL 4X7 *
C6x9-xxx A00AM07677* TUBING, PVC 6X9 *
C7x10-xxx 0779145* TUBING, PVC 7X9 *
EAJ003A
EAJ0003A 6.6-8 COLLAR, MEDIUM D=6-8 1
(1202261003)
3027030
3027030 D7 CLAMP, TUBE D7 1
(1223027030)
EAB041A
E3 FLUID, Y FITTING DI=6.25 1
(1202211041)
EAB028A
FLUID, T FITTING TS7 1
(1202211028)
Sales
Mark on diagram P/n Designation
unit
FITTING, H2O/WASTE CONNECT.ASSY
(Contains: 3 x FITTING, ANTI ROTATION WASHER
XCA196AS
WASTE WASTE H2O EAC008A (1202221008), 3 x FITTING, LUER FEMALE 1
(1209129196)
I=3MM EAC010A (1202221010), 3 x FITTING, LUER
MALE/FEMALE I=2.5 EAC018A (1202221018))
XBA568F
FLUID, WATER STRAW ASSY 1
(1209114568)
XBA574C
FLUID, WASTE STRAW ASSY 1
(1209113574)
LBH004A
FLUID, 10 L CONTAINER 1
(1207791004)
2.2. Valves
V4
V5
A
B
E
F
C
D
V3
V1 V2
V2
V1
3. Temperature control
■A temperature sensor (NTC) measures the temperature within the cooled area of the reagent tray, the
reagent needle or the reaction tray chamber.
■ The error between the setpoint temperature and the measured temperature is calculated.
■ According to the calculated error, the PID controller sends an order to the system. This order is a
percentage of the system cooling or heating capacity.
Controlled
value
Three parameters are used to adjust the PID controller: Gain (Proportional parameter), Ti (Integral
parameter) and Td (Derivative parameter).
The PID controller is adjusted to reach a compromise between:
■a short time of response (determined by Ti)
■a low excess (determined by Td)
■a zero permanent error (ensured by Ti).
For each part (reagent needle, reaction tray chamber and cooled area of the reagent tray), the following
temperature control values are given:
Heading Description
Gain Proportional parameter of PID controller.
Te/Ti Integral parameter of PID controller.
Td/Te Derivative parameter of PID controller.
Te (s) Frequency of the order sent by the PID controller to the system.
For each cycle of a time Te, minimum time on which the signal
Minimum T Off (ms)
amplitude can be at 0.
Assigned Value (°C) Setpoint temperature.
Used for the Manual Mode only.
Assigned Value (%)
Order in % of the cooling or heating capacity.
If checked, the temperature control is manually performed by
Manual Mode
using the Assigned Value in %.
NTC Impedance NTC value for the setpoint temperature.
Current (°C) Measured temperature.
Power (%) Order in % of the cooling or heating capacity.
The order is sent by the PID controller to the system via a PWM (Pulse-Width Modulation) signal.
This PWM signal is proportional to the order in % of cooling or heating system capacity.
The following diagram gives examples of PWM signals in relation with orders in % of cooling or heating
system capacity.
Amplitude
0
0% 25% 50% 75%
Time
0 Te 2Te 3Te 4Te
For each cycle of a time Te, the time on which the signal amplitude is at 0 cannot be lower
than the Minimum T Off. In this case, the time (on which the signal amplitude is at 0) is equal
to 0.
3.2.1. Principle
The reagent tray consists of 52 numbered positions of which 44 are refrigerated and 8 are at room
temperature:
■ Cooled area of the reagent tray, page 3-15
■ Temperate area of the reagent tray, page 3-15.
100%
10% Temperature
14°C 35°C
The fan is activated only if the reagent tray is in its home position (to warm only the temperate
reagent tray area).
Fan
Reagent tray home position:
1- Position 36 in front of the yellow arrow
2- Temperate area in front of the fan
Glycol bath
Evaporator 3
Solenoid valve Capillary
tube
Condenser Dessicator
Compressor
Fan
1 2
■ The refrigerant fluid used in the cooling circuit is a refrigerant gas of R-134 type (Freon).
■ The refrigerant fluid circulating in the cooling circuit undergoes a transformation cycle of four steps.
1. The fluid is in a gaseous state. It passes through the compressor where it is compressed and its
temperature and pressure is raised. Its pressure is then controlled by a pressure sensor (only for
cooling unit CU401).
2. The fluid is in a gaseous state, in high pressure. It circulates through the condenser by a fan where
it passes from a gaseous state into a liquid state and its temperature is slightly reduced. Then, the
fluid circulates through the dessicator (where its impurities are eliminated) before passing through
the capillary tube.
3. The fluid is in a liquid state, in high pressure. It passes through the capillary tube where its
temperature and pressure are reduced. This step is called the gas expansion.
4. The fluid is in the beginning state of a liquid/gaseous transformation, in low pressure. It cools the
glycol bath circulating through the evaporator, where it passes into a gaseous state and its
temperature is slightly raised.
■ The temperature control is performed by the solenoid valve that opens a bypass to inject the hot fluid
into the evaporator.
- If the solenoid valve is opened, the cooling capacity is reduced to zero.
- If the solenoid valve is closed, the cooling capacity rises to its maximum.
■ According to the temperature measured within the cooled area of the reagent tray, the PIC U44 of the
instrument mother board controls the solenoid valve via a PWM signal (Te = 20 s).
3 - 19
Technology
Technology
Temperature control
■ The reagent needle is a stainless steel needle with an external graphitized teflon coating and an internal
sheathing made up of a teflon capillary tube from one end to the other.
■ The reagent needle preheats the reagents at 37°C (± 0.5°C) during the sampling thanks to a resistive
coil wire located along the reagent needle.
The resistive coil wire is powered by 24 V, its resistance is 36 Ω and its electric power is 16 W.
■A temperature sensor (NTC) measures the temperature within the reagent needle.
According to the measured temperature, the PIC U44 of the instrument mother board controls the
heater via a PWM signal (Te = 0.5 s).
■ The PWM signal (5V) is sent from the PIC U44 to the transistor Q3 of the instrument mother board.
Then, the transistor Q3 converts and sends the PWM signal (24V) to power the heater.
■ During the reagent level detection, the reagent needle heater and NTC are respectively switched off
by the relays K1 and K2 of the reagent level detection board in order not to disturb the reagent level
detection.
■ The reaction tray is located in a chamber heated at 37°C (± 0.2°C) thanks to a heater and a fan.
The heater, located at the bottom of the chamber, is powered by 24 V, its resistance is 4.3 Ω and its
electric power is 140 W.
The fan (24 V), located right above the heater, continuously moves hot-air inside the reaction tray
chamber.
■A temperature sensor (NTC) measures the temperature within the reaction tray chamber.
According to the measured temperature, the PIC U44 of the instrument mother board controls the
heater via a PWM signal (Te = 2 s).
■ The PIC U44 of the instrument mother board sends a control signal to the power supply. Then, the
power supply converts the control signal and sends the PWM signal (24V) to power the heater.
Cooled air
Reaction tray NTC
Fan
Heater
Hot air
The reagent level detection is a capacitive level detection and is ensured by the reagent level detection
board. See Section 4: Electric and electronic principles, 3.3. Reagent level detection board, page 4-20.
Depending on the model of the reagent level detection board you have on your instrument, the reagent
level detection principle slightly differs.
Oscillator
U1
Needle
Detector Data treatment Instrument
mother board
NTC Relay K2
Heater Relay K1
Reagent level
detection board
1. The oscillator, built in the microcontroller U1, sends continuously a frequency of 12 MHz to the
reagent needle.
2. When the reagent arm moves down, the instrument mother board sends the following to the
microcontroller U1 of the reagent level detection board:
- the sensitivity level (see Sensitivity level, page 3-23) set according to the liquid to be detected.
- a start signal to start the capacitive level detection.
3. The microcontroller U1 sends a control signal to the relays K1 and K2 which respectively switch off
the reagent needle heater and NTC in order not to disturb the capacitive level detection.
4. The microcontroller U1 sends a shield signal to the heating cable to override the cable noise and the
capacitive effect of the heating cable.
5. The microcontroller U1 measures the voltage variation of the oscillator that directly depends on the
capacitance measured between the reagent needle and the ground.
First, a capacitive measurement is done on air. This measurement gives the reference value.
6. When the reagent needle reaches the liquid, the capacitance as well as the voltage variation change.
7. The microcontroller U1 compares the voltage variation measured with a threshold value. This
threshold value is calculated from the calibration measurement (see Calibration, page 3-23) and the
reference value.
8. A counter counts the number of times the threshold value is overrun. When the counter reaches a
value determined by the sensitivity level (impulsion number), the reagent level detection is effective
(the liquid has been detected).
9. The microcontroller U1 sends a level detection signal to the instrument mother board to stop the
reagent arm movement.
10. The microcontroller U1 sends a control signal to the relays K1 and K2 that switch the reagent needle
heater and NTC on.
11. The microcontroller U1 stops the shield signal.
Sensitivity level
On certain liquids, foam could be created. The sensitivity level avoids the mix up, during the reagent level
detection, between bubbles and liquid. It is determined according to the liquid type and the sampling
location (cassette, rack, etc).
Each sensitivity level corresponds to the number of times the threshold value is overrun before the
reagent level detection is effective.
The instrument mother board sends the sensitivity level in the form of an impulsion number, to the
reagent level detection board.
Number of threshold
Sensitivity level Impulsion number
overrun
Default 0 4
1 1 8
2 2 12
3 3 14
4 4 20
Calibration 7 N/A
Calibration
The calibration determines the reagent needle sensitivity which could vary according to the needle.
It is performed after each reagent needle replacement.
The calibration cycle consists in performing, in the wash tower, a capacitive measurement on air then
on water.
The calibration result gives a reference threshold. This threshold will be compared to the measured
voltage variation during the reagent level detection.
Oscillator U2
Needle U3
Detector Microcontroller Instrument
Data treatment mother board
NTC Relay K2
Heater Relay K1
Reagent level
detection board
1. The oscillator, built in U2, sends continuously a frequency of 240 kHz to the reagent needle.
2. When the reagent arm moves down, the instrument mother board sends the following to the
microcontroller U3 of the reagent level detection board:
- the sensitivity level (see Sensitivity level, page 3-25) set according to the liquid to be detected.
- a start signal to start the capacitive level detection.
3. The microcontroller U3 sends a control signal to the relays K1 and K2 which respectively switch off
the reagent needle heater and NTC in order not to disturb the capacitive level detection.
4. U2 sends a shield signal to the heating cable to override the cable noise and the capacitive effect of
the heating cable.
5. U2 measures the voltage variation of the oscillator that directly depends on the capacitance
measured between the reagent needle and the ground.
First, a capacitive measurement is done on air. This measurement gives the reference value.
6. When the reagent needle reaches the liquid, the capacitance as well as the voltage variation change.
7. The microcontroller U3 compares the voltage variation measured with a threshold value. This
threshold value is calculated from the calibration measurement (see Calibration, page 3-25) and the
reference value.
8. A counter counts the number of times the threshold value is overrun. When the counter reaches a
value determined by the sensitivity level (impulsion number), the reagent level detection is effective
(the liquid has been detected).
9. The microcontroller U3 sends a level detection signal to the instrument mother board to stop the
reagent arm movement.
10. The microcontroller U3 sends a control signal to the relays K1 and K2 that switch the reagent needle
heater and NTC on.
11. U2 stops the shield signal.
Sensitivity level
On certain liquids, foam could be created. The sensitivity level avoids the mix up, during the reagent level
detection, between bubbles and liquid. It is determined according to the liquid type and the sampling
location (cassette, rack, etc).
Each sensitivity level corresponds to the number of times the threshold value is overrun before the
reagent level detection is effective.
The instrument mother board sends the sensitivity level in the form of an impulsion number, to the
reagent level detection board.
Number of threshold
Sensitivity level Impulsion number
overrun
Default 0 25
1 1 50
2 2 100
3 3 200
4 4 400
Calibration 7 N/A
Calibration
The calibration determines the reagent needle sensitivity which could vary according to the needle.
It is performed after each reagent needle replacement.
The calibration cycle consists in performing, in the wash tower, a capacitive measurement on air then
on water.
The calibration result gives a reference threshold. This threshold will be compared to the measured
voltage variation during the reagent level detection.
The calibration result is saved on a flash memory (built in U3) on the reagent level detection board.
A reagent level detection could not be performed if a calibration has not been done.
The sample level detection is a capacitive level detection and is ensured by the sample level detection
board. See Section 4: Electric and electronic principles, 3.2. Sample level detection board XAA486AS
(1209108486), page 4-18. The sample level detection board ensures also the sample shock detection.
Oscillator
PIC U2
Instrument
Needle mother board
Data treatment
Shock detection
switch
Sample level
detection board
1. When the sample arm moves down, the instrument mother board sends a start signal to the PIC U2
of the sample level detection board to start the capacitive level detection.
2. The PIC U2 measures the frequency variation of the oscillator that directly depends on the
capacitance measured between the sample needle and the ground.
3. When the sample needle reaches the liquid, the capacitance as well as the frequency variation
change. The PIC U2 sends a level detection signal to the instrument mother board to stop the sample
arm movement.
The sample shock detection is enabled by the shock detection switch located on the sample arm.
In normal cases, the shock detection switch is in low position: the metal plate keeps the switch in low
position.
In case of shock, the shock detection switch is in high position: the metal plate raises and releases the
switch. The shock detection switch sends a shock detection signal to the instrument mother board to
stop the sample arm movement.
5. Pressure detection
The pressure detection is ensured by two pressure sensors (reagent and sample) located in the syringe
block support and the pressure board located behind the syringe block. See Section 4: Electric and
electronic principles, 5. Pressure board (kit ref. 1300015280), page 4-27.
Signal measurement,
Sample amplification
pressure sensor Result check
and digitisation
1. When the syringes start, the instrument mother board sends a start signal to the pressure board to
start the pressure detection.
2. The pressure board measures the signals (voltages) sent by the pressure sensors (reagent and
sample). These signals directly depend on the pressures measured by the pressure sensors.
3. The pressure board amplifies and digitizes the signals, then sends the results to the instrument
mother board. Two types of results are sent to the instrument mother board:
- results before amplification
- results after amplification.
4. The instrument mother board checks the results to ensure that they are not out of range.
The pressure sensors ensure the detection of the three following troubles:
- High pressure on the sample or reagent hydraulic system (blockage)
- Low pressure on the sample or reagent hydraulic system (water supply failure)
- Bad sampling (fibrin, air bubbles).
Low pressure on the sample or reagent hydraulic system (water supply failure)
During rinsing cycles, the results before amplification are checked to ensure that the pressure is higher
than 300 mbar.
If the pressure is lower than 300 mbar during rinsing cycles, there is a low pressure on the sample or
reagent hydraulic system (water supply failure).
■ Then, the factors KA and KB are applied on the calibration curve on water to determine the low and
high limits of the acceptable range.
y(KA) = KA * (Ax + B)
y(KB) = KB * (Ax + B)
water KA KB
result after amplification
Fibrin
Acceptable range
Air bubbles
volume
During aspirations, the results after amplification are checked to ensure that they are within the
acceptable range.
If they are out of the acceptable range during aspirations, there is a bad sampling (fibrin, air bubbles).
The pressure detection parameters are displayed in the Pressure menu (Services > Diagnostics >
Pressure).
For each pressure sensor (reagent and sample), the following parameters are displayed:
- the high pressure threshold in mbar (A)
- the low pressure threshold in mbar (B)
- the factors A and B of the calibration curve on water as well as the factors KA and KB (C).
Press Set Pressure to calibrate each pressure sensor. At the end of the cycle, the factors A and B of the
calibration curve on water are displayed in the left window.
If the results are correct, press OK to validate the calibration. The new factors are then displayed in the
right window.
If not, press CANCEL to cancel the calibration.
Please refer to the pressure sensors calibration procedure as described in the procedure
RAS442: Pressure sensors, page 1 to calibrate the pressure sensors and make sure that the
results are correct.
Press Read Pressure to display the pressure measured by each pressure sensor at any time. The results
before and after amplification are displayed in the window (D).
If the reading is done when the syringe is not working, the result before amplification should be near 0
and the result after amplification should range between 2000 and 5000. This reading allows you to check
the pressure sensor functioning and the result amplification.
1. Mother board................................................................................................. 4 - 3
1.1. Mother board synoptic .............................................................................................................. 4 - 4
1.2. Mother board configuration ....................................................................................................... 4 - 6
1.3. Mother board adjustments ........................................................................................................ 4 - 7
1.4. Mother board connections ........................................................................................................ 4 - 9
1.5. LEDs on mother board............................................................................................................. 4 - 11
1.6. Mother board Inputs & Outputs ............................................................................................... 4 - 12
8. Connectors .................................................................................................. 4 - 34
8.1. DAC024A (1201891024): CABLE, PRINTER IEEE1284 SHIELD.............................................. 4 - 36
8.2. DAC034A (1201891034): CABLE, CHILLER CABLE ............................................................... 4 - 37
8.3. DAC044A (1201891044): CABLE, USB EXT. CORD L=0.3 M ................................................. 4 - 38
8.4. DAD123A (1201921123): CABLE, PC/PRINT L=1000 5-25 P80 ............................................. 4 - 38
8.5. DAD124A (1201921124): CABLE, PC/RS L=1000 5-09 P80 ................................................... 4 - 39
8.6. DAD134B (1201922134): CABLE, ACQUISIT. BOARD CABLE V1 .......................................... 4 - 40
8.7. DAD134C (1201923134): CABLE, ACQUISIT. BOARD CABLE ............................................... 4 - 41
8.8. DAD135A (1201921135): CABLE, SAMP.RELAY PCB CABLE V1 .......................................... 4 - 42
8.9. DAD135B (1201922135): CABLE, SAMP.RELAY PCB CABLE ............................................... 4 - 43
8.10. DAL029A (1201961029): MOTOR, MIXER ASSY MOTOR .................................................... 4 - 44
8.11. XBA512B (1209112512): CABLE, MOTHER BOARD LEFT CABLE ...................................... 4 - 45
8.12. XBA513C (1209113513): CABLE, RIGHT CABLE ASSY P400 V1......................................... 4 - 47
8.13. XBA513E (1209115513): CABLE, RIGHT CABLE ASSY........................................................ 4 - 48
8.14. XBA514B (1209112514): CABLE, ELECTRO-VALVES .......................................................... 4 - 49
8.15. XBA517D (1209114517): CABLE, DET. BOARD CABLE P400.............................................. 4 - 50
8.16. XBA518A (1209111518): SENSOR, LB TRAY/ARM/MIX/HANDLER ..................................... 4 - 51
8.17. XBA519A (1209111519): SENSOR, LB+MOT.CABLE ARM/HANDL..................................... 4 - 52
1. Mother board
Two mother board references are available depending on the instrument you have:
■ 1300013696 for ABX Pentra 400
■ 1300013697 for Pentra C400
4-4
1.1.
Temperature arm control
1 probe
Photometer amplifier 15 inputs/outputs
Mother board
6 electrovalves
Mixer
RS232 1 step by step motor
1 continuous motor
1 Home sensor
RS232
Host
Printer
Computer
Keyboard
RS232
Screen
Mouse
Electric and electronic principles
Mother board
E1
E8 E3 E2
E4
E5
E7
E6
Jumpers:
1 2 4 3 1
E1 = 1 2 E3 = E5 = E8 =
2 1 3 4 2
E2 = 2 4 E4 = 1 2 E7 = 3 1 E6 = 1 2
1 3 3 4 4 2
Test points and potentiometers are located as shown on the following diagram.
Reaction tray motor Horizontal motions motor Up\Down sample arm Rotation sample arm motor
(R25 - TP1) (R87 - TP9) motor (R224 - TP28) (R227 - TP30)
Mixing motor
(R146 - TP19)
Reagent Syringe motor Reagent Tray motor XY Mixing motor
(R6 - TP2) (R70 - TP11) (R128 - TP16)
Sample Syringe motor Sample Tray motor
(R38 - TP7) (R100 - TP14)
4 - 10
J67 Handling Cuvette
Reagent Syringe home J3 J4 J5 J1
J2 Cover sensor
Mother board
J6
Sample Syringe home J9 Reaction Tray home
J10 J8
Sample Syringe motor Vertical Motion motor
Low position
J53 J54 J51 J52 J55 J56 J57 J58 J59 J50 J60 Sample Arm
Cover Solenoid
Rotation Motor
Waste Water
1.5.
DS8
Compressor Electrovalve
DS11
4 - 11
-5V +5V (+5V) +24V solenoid pump pump Tube / Cup Tube height
DS13 DS14 DS15 DS16 DS12 DS17 DS18 DS7 DS6
Electric and electronic principles
Mother board
GND
4
Water Low Level Switch
PH4
CS_REG_IN 1
2 Fill Tank Switch (NU)
ENEV 3 J28
GND
CPU&GLU CS_REG_OUT CSR5 4
Mixer Position
Arm_switch +24V PH4
D(015) D(015) 1
VCC R241 2
EV(0.6) VCC 10k VCC 1R 3 J29 Reagent Cover Switch
GND
ULNZ003 2 3 4 1 2 3 4 1 R237 4
U33
D(0) 2 19 1 U36 16 11 NI
+24V
UR22
UR22
UR22
UR20
UR20
UR20
UR20
UR22
D0 Q0 LE Waste_Full_SW
D(1) 3 18 2 U36 COM 15 D(0) 19 2 7 6 5 8 7 6 5 8 PH4
D1 Q1 Q0 D0
1 EV(0) D(2) 4 17 3 U36 COM 14 D(1) 18 3 Arms_Cover_SW 1
D2 Q2 Q1 D1
2 D(3) 5 16 4 U36 COM 13 D(2) 12 9 Water_Low_SW 2
D3 Q3 Q2 D2 C182
3 EV(1) D(4) 6 15 5 U36 COM 12 D(3) 13 8 Fill_Tank_SW 3 J30 Arm Cover Switch
Q3
GND
D4 Q4 D3 47p
4 D(5) 8 13 6 U36 COM 11
D(4) 14 7 Reagent_Cover_SW 4
D5 Q5 Q4 D4
5 EV(2) D(6) 9 12 7 U36 COM 10 D(5) 15 6 Arms_Cover_SW
D6 Q6 Q5 D5 GND
COM 16 PC_Wake_up PH4
6 D(7) 7 14 D(6) Q6 5
EV(3) D7 Q7 1 2 3 4 1 3 4 2 D6 1
7 D(7) 17 4 Chiller_Level
J34 Q7 D7
EV Board 8 ENEV 1 OE
1 2
OE
UR27
UR27
UR27
UR27
UR26
UR26
UR26
UR26
GND
9 EV(4) CSR5 11 CLK 3 J62 Hard PC Wake up
8 7 6 5 8 6 5 7 HC573
10 U37 VCC 4
11 EV(5) HC574 10k
GND VCC +24V
12 R151 R161 PH4
EV(6) 470R 470R C213 1
UR29
UR29
UR29
UR29
UR28
UR28
UR28
UR28
CSR5 11 CLK 330R 12
8 7 6 5 8 7 6 5 Barcode 13
R220 R213 10k RxD
C290 VCC U43 CAB_spl_Sensor 14
4k7 4k7 +24V HC574 GND CAB_spl_Sensor
470u VCC Barcode 15
CR3
MURS120 TxD 16
R185 R183 HE10MD16
4k7 4k7 GND
+24V
1 CR2 CR5
DS12 DS17 MURS120 1
J49 2 MURS120
Cover Solenoid Green R214 4k7 2 J55 Waste Pump
R202 R207 D
PH2 Q8 Green C250 C293 C301
BC817 4k7 Q9 HE2
1k IRLL3303 G 100p 100n 100u
R186 S
GND 4k7 GND GND GND
Chiller_Watchdog Chiller_Watchdog
+24V
Chiller On/Off GND
Chiller_Level Chiller_Level
DS18 CR4
Lamp_Stand_By Lamp_Stand_By 1
MURS120
Lamp_ON/OFF Lamp_ON/OFF R215 4k7 2 J56 Water Pump
Power Supply PC_ON/OFF PC_ON/OFF R208
Green D C251 C292 C300
Pwr_Sup_Status Pwr_Sup_Status 4k7 Q10 HE2
IRLL3303 G 100p 100n 100u
VCC R187 S
4k7 GND GND GND
4VCC
3 CHA PHA GND
Optical Encoder J27 2 CHB PHB
1
C455 C456
PH4 GND 100p 100p
Electric and electronic principles
Mother board
4 - 13
GND GND
Electric and electronic principles
Optical acquisition
2. Optical acquisition
The optical acquisition consists in the treatment of the optical signal from the spectrophotometer. This
signal is digitized and sent to the mother board operating system.
BD32 A1_A18
SRAM
MICROPROCESSOR
SPI D0_D15
256 Ko x 16 bits
E CS2 CS7
P
O
T
E
N
T
I ADC BUSY
M
E ADC RD
T
E ADC CONVST
R
OPTICAL AMPLIFIER S CDE MUX
BOARD
D
PRE AMPLI M C
U O
E AMPLI L
T N
T
I V
E
P E
C L R
T E T
O X
E O
R
R R
Application:
■A "TOP_MEASURE" signal is generated at each beginning of a cuvette motion in front of the analysis
window. It is provided by the microprocessor managing the reaction tray. This signal is wired on the
microprocessor level 3 IT.
■ The microprocessor orders, by its I/O ports, the multiplexer to direct the signal of wavelength to
measure to an analogic/numeric convertor.
■ The microprocessor runs a conversion by the activation of the convertor "ADC_CONVST" pin wired in
CS2.
■ When the conversion ends, the convertor picks up the "ADC_BUSY" signal and informs the
microprocessor.
■ The microprocessor receives data (16 bits) by activating the convertor "ADC_RD" pin wired in CS7.
■ At the end of a 100 measurements batch on 2 different wavelengths, the microprocessor generates an
"IT_SPI" signal for the master in order to receive measurement information via the SPI link between
the mother board master microprocessor and the slave microprocessor of the optical processing
board.
■ The amplification gain of each wavelength is adjusted by an E2POT. These E2POTs are commanded
by the microprocessor via an internal SPI bus of the optical processing board.
Microprocessor:
■ Functioning frequency = 25 MHz.
SRAM memory:
■ The SRAM memory is constituted by a housing of 256 Ko x 16 bits. Its selection is performed by the
"CSBOOT" signals of the microprocessor.
To J1 on Optical
Processing Board
The optical processing board XAA483CS (1209109483) is meant to be used on both ABX
Pentra 400 and Pentra C400.
For the ABX Pentra 400, instruments must be equipped with the V5.0.6 software version or
higher.
To J1 on Mother board
3. Level detection
Mother board
10 MHz VCC
The sample level detection board, located on the sample arm, has two functions:
■ level detection: detects the liquid level in different containers (sample tube, sample cup)
■ shock detection: detects possible collision between the sample arm and sample cup bottom or any
other obstacle.
To Sample Needle 1
R3
100k
R4
820k
VCC VCC
VCC
Y1
R5
R1 C1 10MHz 2 GP5/OSC1/CLKIN
4k7
100k 100n
8 3 GP4/OSC2/AN3/CLKOUT
J1 v+ GND
2 GND 4 GP3/MCLR/Vpp
-
1 5 GP2/TOCKI/AN2/INT
3+ Level_detect 6 GP1/AN1/VREF
U1 Start_scan 7 GP0/AN0
4 v- LM393
R2
100k U2
PIC12C672
GND GND
GND 1
2
3
J2
4
5
GND
PH5
D 3.2mm
GND
TP1 (START_SCAN)
TP2 (LEVEL_DETECT)
LEDs function:
■ TheLED DS1 is located between the relays K1 and K2. It gives the state of the relays K1 and K2: the
LED is lit when the reagent needle heater and NTC are switched off.
■ The LED DS2 is located close to the microcontroller U1. It gives the state of the reagent level detection
board: the LED is lit permanently when the reagent level detection board detects a default.
■ The LED DS3 is located under J6. It gives the following information:
- the LED is lit when the reference value on air is acceptable,
- the LED is unlit when the liquid is detected.
DS3
TP2
TP1
U1
DS2
DS1
K2
K1
Components side
To Heating Needle
To J45 on Mother Board
R25
+C18 Q1
U1
D1
C14
U2
D2 K1 J5 J4 J2
A LD2
J1 K2
C12
R20
+C17 TP2
K
+C16 TP1
TP2 LD2
TP1
To J47 on Mother Board
Welding side
Q2
C28
R31
R22
R18
C22
C24 Q4
U4
R19
U3 C20 R26
R30
R33
R23
R24
C21
R28 R29
R21
C26
Q3
LD1
R17
LD1
The component U2 transforms the capacitive value into a voltage. This voltage and its variation around
the threshold voltage are analyzed by the microcontroller U3.
If a variance of voltage is detected (during level detection), the signal "LEVEL_DETECT" pin 5 is put to
"1" and sent to the instrument mother board.
LEDs function:
■ The LED LD1 is located on the welding side close to the microcontroller U3. It gives the following
information:
- the reagent level detection state: it lits during 0.3 seconds when the liquid is detected.
- the reagent level detection board state: if the reagent level detection board detects a default, the LED
is lit permanently.
■ The LED LD2 is located on the components side between the relays K1 and K2. It gives the state of
the relays K1 and K2: the LED is lit when the reagent needle heater and NTC are switched off.
D1 2
U1
1 VOUT CAP+ 5
C12 2
10uF GND
U2 3 CAP-
23 V+ 4
1 LM2767M5
E7 DGND GND LM2767M5
22 3 +
22pF-50V-0603 C29 E6 SHIELDEN
21 4 GND C14 C18
22pF 50V E5 C
20 5 47uF 6V3
22pF-50V-0603 19 E4 B 10uF
2 1 6 GND
22pF
E3 A
18 7 +3.3V
J1 E2 LEVEL C24
GND 17 8 TP1
NEEDLE E1 LPCAP TESTPOINT 2 1 U4
16 9
TEST ROSC S1751-46 1uF-16V-0603 7 IN1 5
15 10 OUT1
GND VDDCAP GND R29
14 11 R33 6K8-1%-0603
SHIELD VPWR 1 8
13 2
2
12 6.8kohm IN2 6
1
AGND VCCCAP R30 OUT2 1 C20
MC3494EG/R2
MC3494EG/R2 1 C21 100nF-16V-0603
MC3494EG/R2 C17 + C16 + 2 4 2
20 kohm
100 ohm
VSSA GND 2 RES GND
20K-1%-0603
2
100R-1%-0603
1
1 3
FB EN
47uF 6V3
47uF 6V3
1nF-16V-0603
R28 TPS77301DGK
GND 3K3-1%-0603 TPS77301DGK GND
R23 TP2 1 2
3.3 kohm
10K-1%-0603 TESTPOINT +5V
1
1 2 2
10 kohm
LEVEL DETECT
1
2 R27 +3.3V 5
2
1uF-16v-0603
D3 47K-1%-0603 GND
C26 1 47 kohm
2 TEST TP_SMD
GND
U3 TP3 R18
1
2 1 GND
2.2kohm
TEST TP_SMD
2
2 1 2 P1.0/TACLK/ACLK/A0
13 GND 1 TP4
XIN/P2.6/TA1 R21
1uF-16v-0603 3 12 X1 TP6 TEST TP_SMD
2.2kohm
P1.2/TA1/A2 TEST/SBWTCK
C25 5 P1.3/ADC10CLK/A3/VREF-/VEREF-
10 GND
+3.3V NMI/RST/SBWTDIO
2 1 6 P1.4/SMCLK/A4/VREF+/VEREF+/TCK
9
P1.7/A7/SDI/SDA/TDO/TDI
1uF-16v-0603 7 P1.5/TA0/A5/SCLK/TMS
8
1 P1.6/TA/A6/SDD/SCL/TDI/TCLK
LD1 MSP430F2012IPW Q3
HSMG-C670 MSP430F2012IPW BC817
2
R17 R26
2K2-1%-0603 R32
1 2 10K-1%-0603
2.2kohm
GND 4K7-1%-0603
1 10 kohm
2 +5V Q4 1 4.7kohm 2
C19 BC817
100nF-16V-0603
+5V
2 1 EH4
1
K1 3 J4 TEMP_FIG
2K2-1%-0603
D2
2
1 +24V
LD2 8 7 6 5 4
BAS516 HEAT_CDE
2 HSMG-C670
GND
2
1 C28
100nF-50V-0603
1
1 2 3 4 2
R20 VSSA
2.2kohm
K2 GND
2K2-1%-0603
EH4
2
D 3.2mm 8 7 6 5
R25 1
10K-1%-0603 2
FX2 FX3 FX1 HEATER
1 10 kohm
2 Q1 3 J5
BC817 4
NTC
Electric and electronic principles
Level detection
4 - 23
GND
GND
Electric and electronic principles
Level detection
On air:
■ Place the reagent arm in "Wash tower position" (above the wash tower).
■ Plug a multimeter in between TP1 and TP2 then check the voltage:
- The voltage must be about 1.9 V (±10%).
On water:
■ Place the reagent arm in "Low Position in Wash" (in the reagent wash tower).
■ Plug a multimeter in between TP1 and TP2 then check the voltage:
- The voltage must be about 1.7 V (±10%).
■ Make sure that the difference between the measurement on air and the measurement on water is
higher than 0.1 V.
To Tube Detector
The sample relay board supplies and transmits information from tube detector (J3), barcode reader (J5),
tube height (not connected J4) and cover LED supply (J2) sensors.
Reflexion sensor
Supply and
J3 info transmission
Tube presence
J4 Supply and
info transmission
Tube height detection
Supply and info transmission
J1 sensors to instrument
mother board
LED
J2
Supply
Cover LED
Supply and
J5 info transmission
Barcode reader
51123
Barcode reader
SAMPLE RELAY BOARD
FACTORY CONFIGURATION:
Jumper Jumper setting
E1 Pin 2 J3 = 0 Short 1 - 2
E1 (Default) Pin 2 J3 = 1 Open WL 160
The pressure board detects fibrin presence or blockage on the sample needle and blockage on the
reagent needle.
After a gain and an offset calibration, the board, according to the pressure on the sensor, digitizes the
analogic signal and sends the digitized information to the instrument mother board.
To ADC µP
P AN1
J1
Offset adjustment
with EEPOT SPI link to
mother board
Microprocessor
16F873
Amplification and
gain adjustment J3
Pressure sensor
Reagent needle
To ADC µP
P AN0
J2
Offset adjustment
with EEPOT
Pressure board
MOTHER
BOARD
To servo-controls
7. Power supply
Two power supply references are available depending on the instrument you have:
■ DBN007E (1202165007) for ABX Pentra 400 with an instrument serial number below 4000
and Pentra C400 with an instrument serial number below 112
■ DBN007F (1202166007) for ABX Pentra 400 since instrument serial number 4000 and
Pentra C400 since instrument serial number 112
The instrument power supply is an AC/DC converter, extensive range input, 8 outputs with power of
450 W maximum.
It provides electrical requirements to the entire instrument except for the cooling unit (independently
connected to the receptacle).
All cables are provided with power supply except the TTL flat cable.
MOTHER BOARD
J53
+ 24 V POWER SUPPLY
VCC FAN
+5V 10 2 J1
MAIN SUPPLY
TB1 TB4 50-60 Hz
+ 5 V, + 12 V, GND
GND V1
ON/OFF FILTER 100-240 Vac
-5V + 24 V V2
FUSES 450 VA
V3: 5 V 2 A
DAC011A
24 V4: 0/5 V 7.2 A (OR DAC012A)
V5-V6: 5/- 5 V 0.5 A
J54 V7: 0/5.1/5.6 V 6.6 A
DZZ039A
PC_On/Off J2
Lamp_On/Off 10 DAD091B CONTROLE
Lamp_Stand by
Power Sup_Status
To servo-controls
This table lists the differences between both power supply references.
7.1. Protection
■ Stop: a stop order cuts the lamp power supply. This functionality is used for an extended analyzer
stand by mode (around few hours).
V2 (+24 V heating) 1
GND 2 P2
Heating module
1 V4 (+5 V computer)
2 V7 (lamp) V7 (lamp) 1
3 V3 (+5 V analyzer) +Sense V7 2 P3
4 V8 (+12 V computer) GND 3
5 -Sense V7 -Sense V7 4 Spectro. lamp
6 V2 (+24 V heating)
7 V1 (+24 V analyzer)
8 GND
9 GND
10 GND
P1 11 GND
Power 12 GND V4 (+5 V computer) 1
13 V4 (+5 V computer) V4 (+5 V computer) 2
Supply 14 V7 (lamp) V8 (+12 V computer) 3
Unit 15 V6 (-5 V analog) 4 P4
16 V5 (+5 V analog) GND 5 Panel computer
17 +Sense V7 GND 6
18 V2 (+24 V heating) GND 7
19 V1 (+24 V analyzer) 8
20 GND
21 GND
22 GND
23 GND V1 (+24 V analyzer) 1
24 GND V1 (+24 V analyzer) 2
V3 (+5 V analyzer) 3
V5 (+5 V analog) 4
V6 (-5 V analog) 5 P5
GND 6 Mother board
GND 7
GND 8
GND 9
GND 10
P1 1 V1 (+24 V analyzer) 1
2 GND EARTH 2 P2
Power Supply Unit 0V 3
EARTH 4 ISE module
Power Supply Unit
Fixing
AWG22-18 Ring Tongue D4
8. Connectors
P50-P51-P52-P66
CCA017A PHR-3 (JST)
Terminals AWG 30-24 M16-M25
SPH-002T-P0.5s
CCA020A
terminals 4161
CAK061A
M44-B46-V50a-V50b-V50c
CCA070A HRP-2 (JST) V50d-V50e-V50f-V50g-V50h
Terminals SHR-001T-P0.6 V51-V64-V66-V66
CCA073A
P16-P25
CAK029A 5102-8
terminals 5103
C21-C29-C33-M35 CAK008A
P35-C39-C41-P57
CCA071A HRP-4 (JST)
P60-CH14
Terminals SHR-001T-P0.6
CCA073A
4-47
8.13. XBA513E (1209115513): CABLE, RIGHT CABLE ASSY
4-48
Electric and electronic principles
Connectors
If the arm cable needs to be replaced on an ABX Pentra 400 V1, please order the KIT,
STRAND TRANSF.ARM & GUIDES XEC166AS (1209179166).
Once you have installed the kit ref. XEC166AS (1209179166) on your instrument, it is not
necessary anymore to order the whole kit to replace the arm cable. Please directly order the
arm cable ref. XBA517D (1209114517).
9. Instrument synoptic
2. Software architecture................................................................................... 5 - 3
2.1. C:\ drive ..................................................................................................................................... 5 - 3
2.2. D:\ drive ..................................................................................................................................... 5 - 5
Main menu
Services menu
Logs menu*
Calibration Applications
Reagent Sequencing
Error Maintenance
System configuration
Application Configuration menu*
Applications
Ratio
Profiles
Customer Services menu* Incompatibility
Cycles Reagents (only for Sales
ISE and Manufacturer)
Analyser
Barcode
Test Counter (available on request)
Diagnostics menu**
System Parameters Spectro
System Configuration menu* Tray Heating
Analyser Audible alarm Arms Sensors
Local Settings Maintenance Syringe Pressure
Host Connection Users Cuvette Changer ISE
Printer Channel configuration (only for Sales) Barcode Test Repeatability
Results validation
2. Software architecture
The instrument hard drive contains two partitions: the C:\ drive and the D:\ drive.
Windows and the instrument software are installed on the C:\ drive.
During the software version installation, the instrument software is installed on C:\Program Files\P400
Software.
The following table describes the most important files of the P400 Software folder.
The following folders are also present in the P400 Software folder.
During the software version installation, the Backup folder is created on the D:\ drive.
You can also find a Bugs folder on the D:\ drive. This folder contains backup copies of the
database and the Error.log file, created when a "GeneralException" error appears.
When the Bugs folder contains a lot of files, software slowness can appear. It is therefore
advisable to suppress these files.
■ Closing the Diagnostics menu, the instrument turns to "Emergency Stop" status. Then,
you have to press Startup to reinitialize the instrument.
■ When you run a cycle from the Diagnostics menu, you must always wait for the end of the
cycle before running another cycle or pressing a new tab.
The System Parameters tab summarizes the instrument parameters (motor adjustments, ...) modifiable
by the technician.
This tab allows you to print, modify, save and restore these instrument parameters.
Moreover, this first tab gives access to the Windows Explorer.
Press Data Print/Send to Host from the generic toolbar to print the list of instrument
parameters displayed in the System Parameters tab.
■ Only the motor adjustments are modifiable from the System Parameters tab.
■ The calibration factors A and B of the sample and reagent pressure sensors and the NTC
value for the reaction tray chamber are not modifiable from this tab; they are respectively
modifiable from the Pressure and Heating tabs.
The backup copies of the instrument parameters are created when you close the
Diagnostics menu and answer OK at the question: "Do you want to save parameters?" (not
necessary if you did not modify the instrument parameters).
3.2. Tray
The Tray tab groups the functions concerning the three trays of the instrument:
- Reagent tray
- Sample tray
- Reaction tray.
For each tray (reagent, sample and reaction), the following functions are available:
Other functionalities:
■ The CAB auto reader adjustment function is used to automatically adjust the reagent tray for the
Reagent Bar Code Reader Position position. To use this function, please refer to the Reagent tray
procedure. See RAS380: Reagent tray, page 1.
■ The Segment function is used to load/unload cuvette segments into the reaction tray:
- automatically using the Load and Unload buttons
- manually using the Forward button.
Sample tray
Position Default value Min. value Max. value
Offset (not modifiable) 80 80 80
Sample Bar code reader Position 316 0 5000
Sample Tube Detector Position 3859 3400 4400
External Sampling Pos. 18568 18100 19000
Internal Sampling Pos. 40 0 19200
Reaction tray
Position Default value Min. value Max. value
Offset 150 50 200
Mixing Position 4755 4000 5000
Reagent Arm Position 948 500 1300
Sample Arm Position (not modifiable) 0 0 0
Automatic Loading 8900 8500 9300
Handling Position 19002 18500 19900
3.3. Arms
The Arms tab groups the functions concerning the reagent and sample arms as the mixer.
Offset Field
See Range of adjustment values for the arm positions, page 5-13.
Position Scrolling list List of the arm vertical positions.
Adjustment value (in number of steps) for the selected position.
Position Field
See Range of adjustment values for the arm positions, page 5-13.
This function is used to automatically adjust the arm vertical
Automatic
Function positions. To use this function, please refer to the Arms procedure.
adjustment
See RAS385: Arms, page 1.
If the arm is at its rotation home position (cuvette position), the light
Colored is green.
Home
square If not, the light is red.
ROTATION
3.4. Syringe
The Syringe tab groups the functions concerning the instrument hydraulic circuit: reagent and sample
syringes, waste and water pumps, valves.
For each syringe (reagent and sample), the following functions are available:
The waste and water pumps can be turned on and off by using the corresponding buttons. Moreover,
the Water pump output function is used to check the water pump output. To use this function, please
refer to the 6 month maintenance procedure. See RAS378: 6 month maintenance, 10. To check the
sample needle throughput, page 8.
The valves can be opened and closed using the corresponding buttons.
Valve Description
V0 Not used.
V1 Sample syringe valve.
V2 Reagent syringe valve.
V3 Mixer wash tower valve.
V4 Reagent wash tower valve.
V5 Sample wash tower valve.
V6 Not used.
The Cuvette Changer tab groups the functions concerning the cuvette changer.
For each cuvette changer motor (vertical motor, horizontal motor, cuvette motion motor), the following
functions are available:
Colored is green.
Home
square If not, the light is red.
The light is gray if the load rack rail position is unknown.
Offset value (in number of steps).
Offset Field See Range of adjustment values for the cuvette changer motor
positions, page 5-18.
Moves the grabber to its vertical/horizontal home position or the
Check Home Button
load rack rail to its home position.
Moves the grabber to the position chosen in the Target scrolling
Check Position Button
list.
Increase/Decrease the adjustment value for the position chosen in
the Target scrolling list.
+/- Buttons
- If you click once, the grabber moves 1/4 of a step.
- If you hold the button down, the grabber moves step by step.
Motor Off Button The selected motor is turned off.
Other functionalities:
■ The Segment function is used to load/unload cuvette segments into the reaction tray:
- automatically using the Load and Unload buttons
- manually using the Forward button.
Horizontal
Cuvette motion
The Barcode Test tab is used to make sure that the reagent and sample barcode readers as well as the
sample tube detector are working correctly.
To use these functions, please refer to the Reagent tray procedure (see RAS380: Reagent tray, page 1)
and the Sample tray procedure (see RAS381: Sample tray, page 1).
3.7. Spectro
The Spectro tab groups the functions concerning the instrument optical bench and spectrophotometer.
The Spectro Measure Adjustment tab is used to adjust the reaction tray home position.
To use this function, please refer to the Reaction tray procedure. See RAS382: Reaction tray, 4.3. Home
position, page 21.
The Spectro Settings and Spectro Measurement tabs are used to check the optical bench and the
spectrophotometer.
To use these functions, please refer to the Optical bench procedure. See RAS383: Optical bench, 4.
Optical bench check, page 31.
3.8. Heating
The Heating tab displays the temperature control values for the reagent needle, the reaction tray
chamber and the cooled area of the reagent tray.
These parameters are described in the Section 3: Technology, 3.1. PID control, page 3-12.
3.9. Sensors
The Sensors tab is used to check the state of several instrument sensors.
Heading Description
If the reagent cover is closed, the light is green.
Handling cover reagent closed
If not, the light is red.
Handling cover reagent locked No check available.
Handling cover cuvette segment If the reaction tray door is closed, the light is green.
closed If not, the light is red.
If the unload rack of cuvette changer is in position, the light is
Rack used segment in position green.
If not, the light is red.
If the unload rack of cuvette changer is full, the light is green.
Rack used segment full
If not, the light is red.
If a cuvette segment is on the load rack, in position to be loaded
New segment available by the grabber, the light is green.
If not, the light is red.
Heading Description
If the water tank is empty, the light is green.
Water tank empty
If not, the light is red.
If the waste tank is full, the light is green.
Waste tank full
If not, the light is red.
Lamp power standby No check available.
If the lamp is running properly, the light is green.
Lamp power full
If not, the light is red.
If the liquid level in the cooling unit is low, the light is green.
Low liquid level (cooling unit)
If not, the light is red.
If the computer wake up push-button is activated, the light is
PC wake up green.
If not, the light is red.
If the arms main cover is closed, the light is green.
Main cover closed
If not, the light is red.
If the mixer assembly is in position, the light is green.
Mixer present
If not, the light is red.
If the power supply is running properly, the light is green.
Power correct
If not, the light is red.
To check the state of these sensors, please refer to the Sensors check and adjustment procedure.
See RAS394: Sensors check and adjustment, page 1.
3.10. Pressure
The Pressure tab is used to configure and calibrate the reagent and sample pressure sensors.
To use these functions, please refer to the Pressure sensors procedure. See RAS442: Pressure sensors,
page 1.
3.11. ISE
The ISE tab groups the functions concerning the ISE module.
This tab is described in the Section 7: ISE module, page 7-1.
3.12. Repeatability
The Repeatability tab is used to perform repeatability cycles on the different instrument mechanical
assemblies to verify that these mechanical assemblies are functioning properly.
Before performing a repeatability cycle, make sure that there is no mechanical assembly in
the way of the mechanical assembly to be checked and move the mechanical assembly to
be checked to its home position:
■ Place the reagent arm in low position in wash tower before moving the sample arm.
■ Move the sample arm to its upper position (vertical home position) before moving the
reagent arm.
■ Move the sample and reagent arms to their upper positions (vertical home positions) before
performing rotation movements.
■ Move the sample and reagent arms to their upper positions (vertical home positions) before
moving any tray.
■ Make sure that the mixer paddle and the cuvette changer grabber are not in low position in
the reaction tray before moving the reaction tray.
During the repeatability cycle, the following information is displayed in the Statistics part (D):
Heading Description
Number of remaining
Number of remaining cycles.
cycles
Number of results Number of rendered results.
Standard Deviation Standard deviation calculated for all the rendered results.
After the repeatability cycle, the results are displayed in the Statistics/Position table (E).
Heading Description
Position Values in 1/16 of a step of the reached positions during the repeatability cycle.
Number of results Number of rendered results per position.
Standard deviation Standard deviation calculated for the rendered results per position.
Coefficient of variation Coefficient of variation calculated for the rendered results per position.
4. Initialization phases
This section describes the different phases of the instrument initialization. If an error appears during
these phases, a warning or an alarm is triggered. See Section 6: Troubleshooting, page 6-1.
2.
■ Boot of the computer
■ Launch of Windows
4. Computer maintenance
■ Version check
■ Database check
■ Language database check
■ Check for archive file creation
■ Result storage capacity check
■ ABX cassette storage capacity check
■ Log storage capacity check
■ Database compacting
7. Login
2. Troubleshooting .......................................................................................... 6 - 42
2.1. Chemistry problem .................................................................................................................. 6 - 42
2.2. Windows and computer error .................................................................................................. 6 - 44
2.3. Cooling unit.............................................................................................................................. 6 - 44
2.4. What to do if you are having intermittent alarms #066 or 114?............................................... 6 - 48
2.5. Other ........................................................................................................................................ 6 - 53
1. Error messages
System warnings and alarms are listed in the following table. See 1.1.1. List of warnings and alarms,
page 6-3.
1. Warnings
Warnings are triggered to warn the user but are not blocking the instrument.
They are displayed on the Warning tab of the System Warnings menu.
When a warning is triggered, the instrument is not stopped but turns to "Ready" status.
If a warning appears, follow the instructions given in the following table. See 1.1.1. List of warnings and
alarms, page 6-3.
2. Alarms
Alarms are blocking the instrument.
They are displayed on the Alarm tab of the System Warnings menu.
The Alarm tab is re-set at each start. To access the previous alarms, press CTRL + F8.
When an alarm is triggered, the instrument is stopped and turns to "Emergency Stop" status.
If an alarm appears, follow the instructions given in the following table. See 1.1.1. List of warnings and
alarms, page 6-3.
6-3
Error messages
Level Code Message Error type / Description Action
6-4
Communication failed on PIC of cuvette
Alarm 016 Cuvette Vertical Motor Initialization Problem
changer vertical motor. Reload the embedded software version on the
Communication failed on PIC of cuvette mother board. See RAS517: Software version
Alarm 017 Cuvette Horizontal Motor Initialization Problem
changer horizontal motor. installation, page 1.
Error messages
6-5
Error messages
Level Code Message Error type / Description Action
6-6
Check the sample arm vertical motion, vertical
Sample arm vertical home position is not
motor connectors.
reached with the acceptable motor
Alarm 032 Sample Vertical Position Error Check the voltages on the mother board: TP28
number of steps (error > 1/2 offset) during
(1 V ± 50 mV), home sensor on J59 Pin1-3 (home
the initialization.
position 5 V, other 0 V).
Error messages
Troubleshooting
6-7
Error messages
Level Code Message Error type / Description Action
6-8
Check the sample needle alignment, the sample
Shock detection switch (SW1) of sample
arm cover.
arm is ON during the initialization, and the
Alarm 046 Shock Detection Out of Service Check the voltage on the sample level detection
sample arm is at its vertical home
board: shock detection switch on J2 Pin2-5
position.
(ON 0 V, OFF 5 V).
Error messages
Troubleshooting
6-9
Error messages
Level Code Message Error type / Description Action
6 - 10
Manually push the mixer down.
Check the "mixer present switch", connector J28
Alarm 065 Mixer not Positioned Detected by the "mixer present switch". on the mother board.
Connector J28 can be disconnected without
triggering any alarm on the instrument.
Error messages
Troubleshooting
6 - 11
Error messages
Level Code Message Error type / Description Action
6 - 12
Check the cuvette changer vertical motion,
vertical motor connectors.
Check the voltages on the mother board: TP6
Cuvette changer vertical home position is
Alarm 111 Cuvette Vertical Motor Position Error (1.2 V ± 50 mV), home sensor (top) on J17 Pin1-3
not reached on time during a run.
(home position 5 V, other 0 V), position detector
Error messages
Troubleshooting
6 - 13
Error messages
Level Code Message Error type / Description Action
6 - 14
Check the sample syringe has no bubble.
Check there is no leaks.
Air detection 2 consecutive times during Check the concerned sample or reagent (level,
sampling, the pressure measured by the foam, bubbles).
Alarm 127 Sample Level Detection Out of Service sample pressure sensor is lower than the Check the low pressure threshold = 300 and factor
Error messages
Troubleshooting
6 - 15
Error messages
Level Code Message Error type / Description Action
6 - 16
See Alarm #136 "Peripheral busy", page 6-34 to
know which motor is concerned by the message.
Alarm 136 Peripheral busy [%s] Incompatible cycle, time out on a motor. Check the concerned motor.
Send to HORIBA Medical the files Asp400bd.mdb
and Error.log for analysis.
Error messages
Troubleshooting
6 - 17
Error messages
Level Code Message Error type / Description Action
6 - 18
Fill the water tank.
Check the voltage of the water tank empty sensor
on the mother board: J31 Pin3-4 (water 0 V, no
Detected by the level switch, located in water 5 V).
Alarm 152 Water Tank Low Level
the water tank. To avoid water level detection alarms when
Error messages
Troubleshooting
6 - 19
Error messages
Level Code Message Error type / Description Action
6 - 20
The sampling alarm SOLUTION_EMPTY/
Check the reagent and replace it if necessary.
SN has been triggered, by the sample
Activate the reagent in the Reagent
Warning 309 SOLUTION_EMPTY/SN on liquid [%s] needle, on the solution [%s] during the
Configuration menu.
shutdown.
Rerun the shutdown.
[%s] = solution short name.
Error messages
Troubleshooting
6 - 21
Error messages
Level Code Message Error type / Description Action
6 - 22
ISE module reagent/fluidic error. LB
sensor cannot detect Standard 1. The LB Check the ISE Standard 1 bottle, hydraulic circuit.
Warning 322 Can’t detect ISE low solution (error code 21) sensor measurement is > 4.5 V (air). Check the valve V4 and readjust the LB sensor.
ISE module status is 4 = module Run an ISE Global Initialization.
sleeping.
Error messages
Troubleshooting
6 - 23
Error messages
Level Code Message Error type / Description Action
6 - 24
The difference between the low and high
standard values is out of the sensitivity Run a 2-point calibration.
ISE electrode [%s1] sensibility error for [%s2] normal range for the electrode in Perform the ISE module maintenance (etching,
Warning 335
point (error code 50) brackets. cleaning).
[%s1] = electrode name. Change the corresponding electrode.
Error messages
Troubleshooting
6 - 25
Error messages
Level Code Message Error type / Description Action
6 - 26
Check the cable from the computer to the mother
Alarm 513 Communication Problem Internal communication failed. board.
Check the power supply on the mother board.
Check the barcode labels on cassettes and
Alarm 514 At least 2 identical Barcodes detected At least two identical reagent barcodes.
Error messages
reagent racks.
Troubleshooting
Problem when configuring the Sample Barcode Sample barcode reader configuration
Alarm 515 Shut down and switch the instrument off and on.
Reader failed.
Problem when configuring the Reagent Barcode Reagent barcode reader configuration
Alarm 516 Shut down and switch the instrument off and on.
Reader failed.
The light intensity on air, measured in the
position 1 of an empty sector of the
Check the optical bench, reaction tray adjustment
Alarm 517 Light intensity out of range reaction tray, is out of the acceptable
and clean the reaction tray.
range (between 57200 and 65535) during
the initialization.
Motor offset value out of range.
Motor [%s1], function position [%s2], value [%s1] = motor name.
Alarm 518 -
[%s3] has changed [%s2] = position name.
[%s3] = old value, new value.
Reinstall the software version. See RAS517:
Bad ISE module version. Software version installation, page 1.
Alarm 519 Bad ISE version Required [%s], Current [%s] [%s] = ISE version number. Reinstall the ISE version on the ISE module. See
Detected during the initialization. RAS540: ISE module software version installation,
page 1.
Spectrophotometer gain check failed.
[%s1] = wavelength.
The lamp has failed the gain check. [%s1 nm / [%s2] = gain.
Alarm 520 Replace the lamp.
%s2 Gain]. Please change the lamp. The gain is out of the acceptable range
(between 1 and 98%) during the
initialization.
Module loading failed.
Check the module connections.
Warning 600 Loading Module [%s]: Not OK [%s] = module name (PRINTER,
Run an initialization.
COMSIL).
Bad language database version.
Language database version [%s] Not OK, version
Warning 601 [%s] = language database version -
required [%s]
number.
6 - 27
Error messages
Level Code Message Error type / Description Action
6 - 28
Fill the water tank.
Check the voltage of the water tank empty sensor
on the mother board: J31 Pin3-4 (water 0 V, no
Detected by the level switch, located in water 5 V).
Warning 610 Water Tank Empty
the water tank. To avoid water level detection alarms when
Error messages
Troubleshooting
6 - 29
Error messages
Level Code Message Error type / Description Action
6 - 30
The sample barcode is not read.
Warning 633 SID [%s1] on position [%s2] not read [%s1] = Sample ID. Check the sample barcode label.
[%s2] = rack position.
The system configuration has been
Error messages
6 - 31
Error messages
Level Code Message Error type / Description Action
6 - 32
Mismatch: Sample [read barcode] was detected For a rack position, the sample ID in the Check the sample.
Warning 655 in [rack position of the sample tube] instead of worklist is different from the read Modify the sample ID in the worklist or move the
expected sample [expected barcode] barcode. sample tube to its correct position.
Error messages
Troubleshooting
This window lists the saved databases (the backup database name and date are displayed).
Each time a new worklist is created, the current database is saved on the instrument. Up to
eight databases are saved and numbered from the most recent to the oldest.
Modifications carried out after this database backup are lost (calibrations, controls, patient
results, reagent consumption, etc.)
# Peripheral
1 Sample arm rotation motion
2 Reagent arm rotation motion
3 Sample arm vertical motion
4 Reagent arm vertical motion
5 Sample syringe motion
6 Reagent syringe motion
7 Sample tray rotation
8 Reagent tray rotation
9 Reaction tray rotation
10 Mixer XY motion
11 Cuvette changer vertical motion
12 Cuvette changer horizontal motion
13 Cuvette motion
14 Temperature regulation
15 Spectrophotometer
16 Pressure sensors
17 ISE module
18 Sample barcode reader
19 Reagent barcode reader
20 Reaction tray temperature
21 Reagent tray temperature
22 Reagent needle temperature
Time of
Code Type Message Acceptable range
stabilization
The stability was not reached during the instrument initialization.
053 ALARM Reaction Tray Temperature regulation failed 37°C (+/- 0.25°C) < 15 min.
054 ALARM Heating Needle Temperature regulation failed 37°C (+/- 1.5°C) < 10 min.***
Refrigerated Compartment Temperature
055 ALARM 4-10°C < 4 hours*
regulation failed
The stability was reached during the instrument initialization but the temperature is now out of range.
123 WARNING Reaction tray temperature exceeds limits 37°C (+/- 0.25°C) < 2 min.
053 ALARM Reaction Tray Temperature regulation failed 37°C (+/- 0.5°C) None
124 WARNING Heating needle temperature exceeds limits 37°C (+/- 1.5°C) < 24 sec.
054 ALARM Heating Needle Temperature regulation failed 37°C (+/- 3°C) None
305 WARNING Reagent tray temperature exceeds limits** 4-10°C < 30 min.
Refrigerated Compartment Temperature
055 ALARM 2-12°C None
regulation failed
* Every hour from the start of the cooling unit, the temperature in the refrigerated area of the
reagent tray (if it is still out of the acceptable range) is checked to ensure that it is decreasing
by at least two degrees per hour. If not, the alarm #055 "Refrigerated Compartment
Temperature regulation failed" is triggered.
** Before performing the analyses, the reagent tray temperature is checked and if it is out of
range, a dialog box is displayed: "The current reagent tray temperature [temperature] is out
of the range (acceptable range). The results can be affected by this malfunction. We
recommend you to perform controls. Do you still want to run analysis?".
*** On each start of the heating needle temperature regulation, a test period of 5 seconds is
performed. This test period consists in heating at its maximum power within 5 seconds, then
checking that the temperature has increased by at least 1.5°C.
If the temperature has increased of 1.5°C or more, then the heating needle temperature
regulation works properly. If not, the alarm #142 "Reagent Needle Temperature Sensor Out
of Order" is triggered and the heating needle temperature regulation is stopped.
■ After five minutes, the cooling unit operation is back to normal. If a new "Compressor overload" alarm
is triggered, it is considered as the first one.
6 - 37
Error messages
Troubleshooting
Error messages
Sampling alarms are displayed on the Sampling Exception tab of the Test Review menu.
If a sampling alarm is triggered, follow the instructions given in the following table.
6 - 39
Error messages
Message Error type Action
6 - 40
Check the sample.
For a rack position, the sample ID in the worklist is different from the read
MISMATCH Modify the sample ID in the worklist or move the
barcode (Sampling status).
sample tube to its correct position.
Air bubbles or insufficient volume (detected by the sample pressure sensor).
INC_SAMPLE_PIPET Check the sample.
Error messages
6 - 41
Error messages
Troubleshooting
Troubleshooting
2. Troubleshooting
This guide is intended to provide help in solving problem situations that may appear when using the
instrument.
The actions described in this troubleshooting chapter must be undertaken if all the user troubleshooting
steps, described in your user manual (refer to the "Maintenance and Troubleshooting" chapter), have
been performed.
For any situations that cannot be resolved by using this guide, please contact the International Technical
Support department (ITS).
Services and repairs of the instrument should only be carried out by a fully trained technician.
In all cases, first perform the "Precision test" procedure. See RAS393: Check up after intervention,
page 1.
2.1.1. Repeatability
1. Test T1 or P1 with CV > 1%
Cause Action
Worn syringe plunger tips. Change the syringe plunger tips.
Check the mixer paddle rotation, coupling, position.
Improper mixing.
Check the mixer XY motion.
Clean the hydraulic system with bleach solution.
Defective manifold, valves V1 or V2.
Change the manifold block.
Check the straw position into the water tank.
Bubbles in the pipetting system. Check the airtightness of the hydraulic system.
Change the manifold block, water pump.
Bubbles clung to the syringe plunger tips. Change the syringe plunger tips.
Prime the hydraulic system.
Clogged sample needle.
Change the sample needle.
Bubbles on the top of sample. Remove the bubbles.
Lamp instability. Change the lamp.
Cause Action
Use new ABX Pentra Qualitest Solution or ABX Pentra
Contaminated or expired solution.
Precitest Solution, use fresh distilled water on the rack.
Manually dilute the control solution and measure the
absorbance value in the Spectro menu.
- Test T1: 2.5 µL of ABX Pentra Qualitest Solution + 587.5 µL
of distilled water
Defect on the spectrophotometer or
- Test P1: 3 µL of ABX Pentra Precitest Solution + 292 µL of
pipetting.
distilled water
If the absorbance value x 1000 is in the acceptable range,
then there is a defect on the pipetting. Otherwise, check the
spectrophotometer.
Cause Action
Check the distilled water integrity, resistivity > 5 Mohm.cm
Contaminated distilled water and tubing.
Perform the decontamination procedure.
Contaminated or expired reagent. Use fresh reagent.
Use of cuvette segments non-approved
Use HORIBA Medical approved cuvette segments.
by HORIBA Medical.
Re-used cuvette segments. Cuvette segments are designed for single use only.
Cause Action
Check the distilled water integrity, resistivity > 5 Mohm.cm
Contaminated distilled water and tubing.
Perform the decontamination procedure.
Contaminated or expired calibrator,
Use fresh calibrator, reagent.
reagent.
Bubbles/foam on the top of reagent (on
Remove the bubbles/foam.
cassette or reagent rack).
For kinetic tests, temperature regulation Check the reaction tray temperature regulation.
problem. Change the reaction tray temperature sensor.
For user channels, not suitable calibration
factor limits in the application Redefine the calibration factor limits.
configuration.
Cause Action
Error in the confidence range
Check the configured values with the corresponding annex.
configuration.
Recalibrate with fresh calibrator.
Expired calibration, reagent.
Replace the reagent and recalibrate.
Error Action
Shut down and restart the computer. Perform a Checkdisk.
Purge the Rs_Data and Bugs folders.
General exception
If the error continues to appear, reinstall the software
version.
Boot disk failure Reinstall the Windows master and the software version.
"CLAC"
■ From the Heating menu (Services >
Diagnostics > Heating), press Start and
check by ear if the solenoid valve has
switched ("CLAC").
Cable defective?
■ Check the cable conductivity with an ohmmeter (see Section 4: Electric and electronic principles, 8.2.
DAC034A (1201891034): CABLE, CHILLER CABLE, page 4-37).
Pump is running?
This troubleshooting guide is intended to help you in solving problems of intermittent alarms #66 or
#114: "Low pressure on the Sample or Reagent hydraulic system". We recommend performing the
following steps in the indicated sequence:
■ 2.4.1. Pressure sensors activation, configuration, calibration, page 6-48
■ 2.4.2. Improving the hydraulic system airtightness, page 6-50
■ 2.4.3. Checking the sample needle throughput, page 6-52
■ 2.4.4. Checking the water pump pressure, page 6-52
■ 2.4.5. Replacing the pressure sensors and the pressure board, page 6-52
Both pressure sensors must be activated. Otherwise, erroneous test results could occur.
7. Make sure that no air bubbles are visible in the syringes and check for leaks.
In case of problem, check the syringe plunger tips, the syringes and the manifold assembly (V1-V2).
If you are still having intermittent alarms #66 or #114, go to 2.4.3. Checking the sample needle
throughput, page 6-52.
If you are still having intermittent alarms #66 or #114, go to 2.4.4. Checking the water pump pressure,
page 6-52.
If you are still having intermittent alarms #66 or #114, go to 2.4.5. Replacing the pressure sensors and
the pressure board, page 6-52.
2.5. Other
Cause Action
Use of cuvette segments non-approved
Use HORIBA Medical approved cuvette segments.
by HORIBA Medical.
Re-used cuvette segments. Cuvette segments are designed for single use only.
Check the lamp voltage (5.6 V).
Lamp instability.
Change the lamp.
Dirty optical bench lenses. Clean the optical bench lenses.
Cause Action
Bad adjustment of the barcode reader. Readjust the barcode reader.
Bad barcode label. Check the barcode label with the supplier.
2.5.3. No sound
Cause Action
Incompatible software version. Install the latest higher software version.
Incompatible hardware. Install the KIT, SOUND+USB UPDATE KIT P400.
Check the loudspeaker connectors.
Defective loudspeaker.
Change the loudspeaker.
3. Procedures .................................................................................................. 7 - 42
3.1. Maintenance by customers .....................................................................................................7 - 42
3.2. ISE 6 month maintenance ........................................................................................................7 - 42
3.3. ISE yearly maintenance ...........................................................................................................7 - 42
3.4. ISE procedure list ....................................................................................................................7 - 43
3.5. ISE maintenance check up summary ......................................................................................7 - 43
RAS441: ISE module installation
RAS388: ISE module maintenance
RAS537: ISE module check up after intervention
RAS538: ISE module spare part replacement
RAS539: Dummy PENTRA software use
RAS540: ISE module software version installation
The measurement principle is based on the interaction between moveable free ions in a sample solution
and an active sensing unit (ion selective sensing electrode).
An ion-selective membrane separates the sample solution, where the electrolyte concentration is
unknown, from the electrode electrolyte, where the concentration is known.
Potentiometry principle
Voltage measurement
Electrolyte
(known concentration) Selective membrane
- -
+ + +
+ -
- - -
- + -
-
+ + + +
- + +
-
The membrane itself consists of a specific type of material which can react with one type of ions.
The four electrodes are compact and located in a Faraday cage to minimize the influence of electro-
magnetic fields.
This electrode layout allows a simultaneous measurement of the Na+, K+ and Cl- concentration.
The electrodes are supplied ready for use and no assembly is required.
Sealing-ring
Sealing plug
Sealing plug
O-ring
O-ring
Electrode
Electrode
Electrolyte
Electrolyte
Electrode body
Electrode body
PVC crown
ether membrane
Plastic membrane
O-ring
O-ring
The electrode membrane can bind a selective type of ions whereby a potential change appears at the
membrane/sample boundary.
Membrane
Ion selective
membrane
+ + + + +
+
+ +
Δ mV + + +
+
+ + +
+ + Sample +
In order to measure this potential change, a reference electrode with a fixed potential is immersed in the
same solution. The potential of the reference electrode is kept fixed and constant, by filling it with an
electrolyte that has a constant concentration.
The electrical potential is measured between each ion selective electrode and the reference electrode.
This measured potential is proportional to the ion concentration.
STD1
STD2
Low Waste Ref. High
Syringe 1 Syringe 2
VOLTMETER
Air sensor
Ref Na Cl K
REF
Cup
The potential values ascertained are amplified, digitized and finally sent via the RS232C serial interface
to the instrument.
1.1.2. Calibration
The calculation of the ion concentration in a sample solution is derivated from a calibration curve.
When carrying out a calibration, the ion selective electrodes and the reference electrode are brought in
contact with a series of solutions (standards) with known concentration.
The voltages are recorded. The concentration of each standard is plotted against the measured voltage
(in millivolts) on semi-logarithmic paper. The straight line drawn through these points is called a
calibration curve.
mV K+ = 37 to 67 mv/dec
K+
Cl-
Na = 38 to 65 mv/dec
Na
CONCENTRATION
Std1 Std1 Std1 Std2 Std2 Std2
The electrical potential measured between these electrodes is proportional to the concentration of the
specific ion, and can be described by the Nernst equation:
E = E0 + S * log ai
where:
E: Measured potential between ion selective electrode and reference electrode
E0: Standard potential of electrode assembly
S: Electrode slope (Nernst factor)
ai: Activity of measured ion
The S slopes of the three electrodes are determined with two standard solutions of known
concentration.
The cycles described on the following pages correspond to the ISE software version V1.53
for the ABX Pentra 400 or V2.00 for the Pentra C400.
Caption
Item Definition
Std1 ABX Pentra Standard 1, ref. A11A01717
Std2 ABX Pentra Standard 2, ref. A11A01718
R ABX Pentra Reference 280 mL, ref. A11A01901
S1Mx Measured potential of Standard 1
S2Mx Measured potential of Standard 2
RM Measured potential of Reference solution
CSx Known concentration of Standard
SM Measured concentration of sample (serum, plasma)
UM Measured concentration of diluted sample (urine + Standard 1)
S:x ISE module status at the beginning and at the end of the cycle
W:x Warning
Global initialization
mV
Initialization of
Two point calibration
flow system
Std1/Std2/R Std1/Std2
1 2
t
S:0,1,2,3,4,5,6 S:6
1. The ISE module initializes the flow system (see Initialization of the flow system, page 7-7).
2. A two point calibration is run (see Two point calibration, page 7-8).
mV Reagent detection
Rinsing
(x4) Rinsing
Reagent detection
+ Keep condition in electrode
Rinsing
(x6) Rinsing Rinsing
Std1 Std1 Std1
1 2 3 4 5 6 t
S:3,4,5,6 S:5
1. Rinsing with Reference (4 times): Reference solution passes through the reference electrode then
goes to waste.
2. Rinsing with Standard 2 (4 times): Standard 2 is dispensed into the ISE sample cup, passes through
the electrode then goes to waste.
3. Rinsing with Standard 1 (6 times): Standard 1 is dispensed into the ISE sample cup, passes through
the electrode then goes to waste.
4. Rinsing with Standard 2: Standard 2 is dispensed into the ISE sample cup, detected by the LB sensor
then goes to waste.
During liquid check by the LB sensor, if Standard 2 is too much or not enough, warning #327 or #330
is triggered. The cycle is stopped.
5. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
6. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode (keep condition). The end of the aliquot is detected by the LB sensor.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
mV
W:338
S2M1
W:335
1 2 3 4 5 6 7 8
t
S:4,5,6 3 sec. S:6 or 4 (if 4 at the beginning)
3 sec.
4. Rinsing with Standard 1: Standard 1 is dispensed into the sample cup, passes through the electrode
then goes to waste.
The slope in sensitive electrode is calculated from the values of the Standard 2 measurement (S2M1)
and the third measurement of Standard 1 (S1M3):
6. Rinsing with Standard 1: Standard 1 is dispensed into the sample cup, passes through the electrode
then goes to waste.
7. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
8. Third measurement of Standard 1 (S1M3): this measurement is rerun to check the correct functioning
of the valves. The S1M3 is rerun maximum 6 times.
mV
Reagent detection Keep condition in electrode
1 2 3
t
1. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. The end of the aliquot is detected by the LB sensor. Standard 1 goes to waste.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
3. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
mV
W:338
Reagent
W:337
detection Keep condition in electrode
S1M2
S1M X6 max.
Rinsing S1M1 Rinsing
Std1 Std1
1 2 3
t
S:4,5,6 3 sec. S:identical to the initial status
1. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
3. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
Serum measurement
mV
W:338
SM
Serum/Plasma
(50 µL)
Reagent detection
+ Keep condition
in electrode
W:338
Rinsing S1M1
Std1 Std1
1 2 3
t
S:6 3 sec. 3 sec.
S:6
1. Sample measurement:
- 60 µL of sample (serum, plasma) is pipetted by the sample needle and 50 µL is dispensed into the
ISE sample cup.
- The sample is aspirated in the electrode. The end of the aliquot is detected by the LB sensor.
During liquid check by the LB sensor, if sample is too much or not enough, warning #331 or #334 is
triggered.
The cycle is skipped to the rescue cycle (see Serum measurement rescue cycle, page 7-12).
- The sample concentration is measured.
If the difference in potential during the last 3 seconds of measurement is ≥ 0.40 mV, warning #338
("ISE Error") is triggered.
- Sample goes to waste.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
The sample concentration is calculated from the values of the measured concentration of sample
(SM), the measured potential of Standard 1 (S1M) and the slope obtained in the two point calibration.
Dilution concentration = CS1 x 10^((SM-S1M)/Slope)
Where:
- SM is the measured concentration of sample
- S1M is the measured potential of Standard 1
- Slope comes from the two point calibration
- CS1 is the known concentration of Standard 1
mV
1
t
1. Measurement of Standard 1 (S1M):
- Standard 1 is dispensed into the ISE sample cup, then aspirated in the electrode. The end of the
aliquot is detected by the LB sensor.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
- The potential of Standard 1 is measured.
If the difference in potential between the current S1M and the previous S1M is ≥ 0.40 mV, the rescue
cycle is rerun (max. 6 times) after updating the previous S1M to the current S1M. If it is more than 6
times, warning #337 is triggered. The cycle is stopped.
- Standard 1 stays in the electrode (keep condition).
Urine measurement
mV
W:338
UM
Urine (10 µL)
+
Std1 (60 µL)
Reagent detection
+ Keep condition in electrode
W:338
Rinsing Rinsing Rinsing Rinsing S1M1
Std1 Std1 Std1 Std1
1 2 3 4 5 6
t
S:6 3 sec. 3 sec.
S:6
1. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
2. Sample measurement:
- 60 µL of Standard 1 is dispensed into the ISE sample cup. An air bubble is created (LV6
commutation and small aspiration by syringe 1). Then, LV6 commutes and Standard 1 is dispensed
(through the top connector) into the ISE sample cup. This cycle will avoid contamination between
Standard 1 and mixing solution.
- 20 µL of sample (urine) is pipetted by the sample needle. 10 µL is dispensed into the ISE sample
cup and diluted with Standard 1.
- The sample is aspirated in the electrode. The end of the aliquot is detected by the LB sensor.
During liquid check by the LB sensor, if sample is too much or not enough, warning #331 or #334 is
triggered.
The cycle is skipped to the rescue cycle (see Urine measurement rescue cycle, page 7-14).
- The sample concentration is measured.
If the difference in potential during the last 3 seconds of measurement is ≥ 0.40 mV, warning #338
("ISE Error") is triggered.
- Sample goes to waste.
3. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup (from the LV6- inlet 3 to
the middle inlet of the ISE sample cup), passes through the electrode then goes to waste.
4. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup (from the LV6- inlet 1 to
the upper inlet at the back of the ISE sample cup), passes through the electrode then goes to waste.
5. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup (from the LV6- inlet 3 to
the middle inlet of the ISE sample cup), passes through the electrode then goes to waste.
The sample concentration is calculated from the values of the measured concentration of diluted
sample (UM), the measured potential of Standard 1 (S1M) and the slope obtained in the two point
calibration.
Dilution concentration = CS1 x 10^((UM-S1M)/Slope)
then,
Concentration = 7 x Dilution concentration - 6 x S1M
Where:
- UM is the measured concentration of the diluted sample
- S1M is the measured potential of Standard 1
- Slope obtained from the two point calibration
- CS1 is the known concentration of Standard 1
mV
1
t
1. Measurement of Standard 1 (S1M):
- Standard 1 is dispensed into the ISE sample cup, then aspirated in the electrode. The end of the
aliquot is detected by the LB sensor.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
- The potential of Standard 1 is measured.
If the difference in potential between the current S1M and the previous S1M is ≥ 0.40 mV, the rescue
cycle is rerun (max. 6 times) after updating the previous S1M to the current S1M. If it is more than 6
times, warning #337 is triggered. The cycle is stopped.
- Standard 1 stays in the electrode (keep condition).
mV
Rinsing Rinsing
R Std2
Reagent detection
Reagent detection + Keep condition in electrode
1 2 3 4 5 6 7
t
S:4,5,6 S:5
1. Rinsing with Reference: Reference solution passes through the reference electrode then goes to
waste.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
3. Rinsing with Standard 2: Standard 2 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
4. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
5. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. The end of the aliquot is detected by the LB sensor. Standard 1 goes to waste.
6. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
7. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode (keep condition). The end of the aliquot is detected by the LB sensor.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
Draining
mV
Rinsing
(x6)
Rinsing Std2
(x4)
R
Rinsing
(x6)
Std1
1 2 3
t
S:3,4,5,6 S:3
1. Rinsing Reference (4 times): Reference solution passes through the reference electrode then goes to
waste.
2. Rinsing with Standard 2 (6 times): Standard 2 is dispensed into the ISE sample cup, passes through
the electrode then goes to waste.
3. Rinsing wih Standard 1 (6 times): Standard 1 is dispensed into the ISE sample cup, passes through
the electrode then goes to waste.
Cleaning
mV
Reagent detection
Cleaning twice
+ Waste
Rinsing
Cleaning
solution Std2
(80 µL)
Reagent detection
+ Keep condition in electrode 4 times
Rinsing
Std1
1 2 3
t
S:4,5,6 S:identical to the initial status
1. Cleaning with cleaning solution: 80 µL of cleaning solution is dispensed into the ISE sample cup, then
aspirated in the electrode for cleaning. The end of the aliquot is detected by the LB sensor. Then, it
goes to waste.
During liquid check by the LB sensor, if the cleaning solution is too much or not enough, warning
#331 or #334 is triggered. The cycle is skipped to step 2.
2. Standard 2 is dispensed into the ISE sample cup, then aspirated in the electrode (keep condition).
The end of the aliquot is detected by the LB sensor. Then, it goes to waste. (twice)
During liquid check by the LB sensor, if Standard 2 is too much or not enough, warning #327 or #330
is triggered. The cycle is stopped.
3. Standard 1 is dispensed into the ISE sample cup, then aspirated in the electrode (keep condition).
The end of the aliquot is detected by the LB sensor. (4 times)
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
Wake up
mV
Stabilization of
flow system Two point calibration
R/Std2/Std1 Std1/Std2
1 2
t
S:4,5,6 S:6
1. The ISE module stabilizes the flow system (see Stabilization of flow system, page 7-15).
2. A two point calibration is run (see Two point calibration, page 7-8).
Keep ready
When the instrument is shut down and to keep the electrodes stability, the ISE module runs the "Keep
ready" cycle to ensure reagent transfer at electrodes level.
Frequency: every 15 minutes (can be modified by the user, see ISE calibration setting, page 7-30).
mV
Reagent detection Keep condition in electrode
Rinsing Rinsing
Std1 Std1
1 2
t
S:4,5,6 S:4
1. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. The end of the aliquot is detected by the LB sensor. Standard 1 goes to waste.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
Ready
When the instrument is in operation and to keep the electrodes stability, the ISE module runs the
"Ready" cycle to ensure reagent transfer at electrodes level.
Frequency: every 5 minutes (can be modified by the user, see ISE calibration setting, page 7-30).
mV
Reagent detection Keep condition in electrode
Rinsing Rinsing
Std1 Std1
1 2
t
S:6 S:6
1. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. The end of the aliquot is detected by the LB sensor. Standard 1 goes to waste.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
Activation
The activation cycle consists in running one serum or plasma sample to condition electrodes.
mV
Detection
+ Keep condition in electrode
+ Waste
Sample
Reagent detection Keep condition in electrode
(50 µL)
1 2 3 4
t
S:4,5,6 S:identical to initial status
1. 60 µL of sample (serum, plasma) is pipetted by the sample needle and 50 µL of serum or plasma
sample is dispensed into the ISE sample cup. Sample is detected by the LB sensor, stays in the
electrode (keep condition) then goes to waste.
During liquid check by the LB sensor, if sample is too much or not enough, warning #331 or #334 is
triggered. The cycle is skipped to step 2.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, passes through the
electrode then goes to waste.
3. Standard 1 is dispensed into the ISE sample cup, then aspirated in the electrode. The end of the
aliquot is detected by the LB sensor. Standard 1 goes to waste.
During liquid check by the LB sensor, if Standard 1 is too much or not enough, warning #322 or #325
is triggered. The cycle is stopped.
4. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
Shut down
1 2
t
S:3,4,5,6 S:3
1. Rinsing with Reference: Reference solution passes through Reference electrode then goes to waste.
2. Rinsing with Standard 1: Standard 1 is dispensed into the ISE sample cup, then aspirated in the
electrode. Standard 1 stays in the electrode (keep condition).
Electrode replacement
mV
Waste
Std1
1
t
S:3,4,5,6 S:Not applicable
mV
S1M
1
t
S:3,4,5,6 S:3 or 4
mV
S2M
1
t
S:3,4,5,6 S:3 or 4
mV
RM
1
t
S:3,4,5,6 S:3 or 4
LB sensor check
mV
LB sensor detection
+ Keep condition in electrode
Std1
1
t
S:3,4,5,6 S:3 or 4
1. Standard 1 is dispensed into the ISE sample cup, then aspirated in the electrode. The end of the
aliquot is detected by the LB sensor.
If the LB Sensor cannot detect "ON" or "OFF", warning #322 or #325 is triggered.
The ISE module exists in seven different statuses. While the instrument is running, the status of the ISE
module is displayed in the ISE tab. Go to Services > Customer Services > ISE.
The status from 0 to 6 of the ISE module are described in the following table:
Code Description
0 Module not initialized
1 Module initialized
2 Module configured
3 Mechanical part initialized
4 Module sleeping
5 Fluidic part initialized
6 Module calibrated
In correct working order, the ISE module evolves sequentially from status 0 to 6, thus from the instrument
start up (Power ON) to the calibrated module achievement, ready for the analyses.
This diagram is available in the form of a sticker to be stuck on the inside of the ISE cover:
STICKER, ISE HYDRAULIC HAX0271 (1207230271).
Fuse
To power supply
To the analyzer
To Reference electrode
TP3
To Reference electrode
To Cl electrode TP2
To K electrode
ISE software board CPU-03N XAA497E (3200448459) for ABX Pentra 400 only
ISE software board CPU-07N XAA646A (3200375620) for Pentra C400 only
CPU-03N (P400) /
CPU-07N (PC400)
Reference
Amplifier RS232
electrode Peripheral
control circuit
Na
Amplifier RS-232C-2
electrode
MPX Signal
AD converter isolator
Cl
electrode Amplifier
Syringe-1
Syringe-1
drive circuit
LB
sensor Amplifier
Syringe-2
Syringe-2
drive circuit
(DC 5 V)
(DC 5 V) DC/DC
converter
Power supply
(DC24V)
DC/DC
converter
Valves
To power
supply
Valves
7 - 27
ISE module description
ISE module
ISE module description
To minimize environmental interferences, the ISE module cover must always be closed during
ISE module operation.
ISE Module
Status button
Pentra C400
ISE Module
Status button
ISE module not initialized. ISE module needs to be activated. See ISE customer
services screen, page 7-30.
A B
An electrode cannot be inactivated if there are ISE tests for this electrode in the worklist or
for validation.
■ Change electrode:
Helps the user to replace an electrode.
The ISE module drains the reagents from the electrodes to allow the user to replace the electrode.
The ISE module will be stabilized in status 4.
The Change electrode key is enabled only if the ISE module is not occupied and its status ≥ 3.
■ Fluidic Initialization:
Primes the reagents into the fluidic system.
This function should be used after the ISE reagents replacement or an ISE shutdown (complete stop of
the ISE module) exceeding three days.
The Fluidic Initialization key is enabled only if the ISE module is not occupied and its status ≥ 3.
■ Drain:
Drains the reagents from the fluidic system.
This function should be used for an ISE shutdown (complete stop of the ISE module) exceeding three
days or the system transportation.
The Drain key is enabled only if the ISE module is not occupied and its status ≥ 3.
■ Global Initialization:
Initializes the ISE module.
The Global Initialization key is enabled only if the ISE module is not occupied.
■ Mechanical Initialization:
Checks the syringe movement and sets the syringes to their initial position.
The Mechanical Initialization key is enabled only if the ISE module is not occupied and its status ≥ 2.
■ Shutdown:
ISE shutdown (complete stop of the ISE module) exceeding three days. See 1.6.3. ISE module
shutdown, page 7-32.
Fills the electrodes with low standard and air to prevent the contamination of the reference solution.
The Shutdown key is enabled only if the ISE module is not occupied and its status ≥ 3.
C A
After opening, ISE reagents are stable for one month if stored at 5-30°C and protected from
light.
Store the electrodes in a dry and clean area in their original packaging.
To use those functions, select the corresponding option and press Check.
If the function is correct, the corresponding light becomes green.
■ Global Check:
Checks all the elements of the ISE module for example the mechanical movement of the syringes and
valves.
This command is a batch of "Standard 1", "Standard 2", "Sample Detection", "Needle 1 Liquid
Aspiration", "Needle 2 Liquid Aspiration", "Valve Check", "LB Sensor", "Cleaning", and "Keep ready"
functions.
■ Sample Detection:
Checks the correct functioning of the sample detection.
■ ValveCheck:
Checks the liquid valves movement (open then close the four valves).
■ LB Sensor:
Checks the correct detection between air and liquid.
■ Cleaning:
Commands ISE module cleaning.
■ Keep ready:
Maintains liquid (Standard 1) in the fluidic system during the shutdown.
■ Global Initialization:
Initialization of the system, which is a batch of "Request status" (sets status, the instrument obtains the
current status), "Request Data" (sets data, the instrument obtains the current data), "Mechanical System
Initialization", "Prime flow system" (primes the reagent into the fluidic system; rinses the distilled/
deionized water into the fluidic system) and "Two point calibration" functions.
■ Data Initilization:
Initialization of the ISE module data.
If a function is used (except Cleaning cycle), you must run a Global Initialization before
leaving this menu.
■ Messages:
Displays the ISE error messages of previous tests (see 2. Error messages, page 7-38).
Total consumption
NA: 0.2 mv
K: 0.3 mv
CL: 0.2 mv
NA: 38 to 65 mv
K: 37 to 67 mv
CL: -53 to -28 mv
Standards concentration
Standard 1 Standard 2
NA: 120 meq 200 meq
K: 4 meq 7 meq
CL: 100 meq 150 meq
Cycle Condition
Two point calibration Executed every 2 hours (except when the instrument is shut down)
One point calibration Executed every 15 minutes (except when the instrument is shut down)
Ready Executed every 5 minutes (only when the instrument is running)
Keep ready Executed every 15 minutes (only when the instrument is shut down)
2. Error messages
System warnings and alarms are listed in the table on the following pages.
1. Warnings
Warnings are triggered to warn the user but are not blocking the instrument.
They are displayed on the Warning tab of the System Warnings menu.
When a warning is triggered, the instrument is not stopped but turns to "Ready" status.
If a warning appears, follow the instructions given in the table on the following pages.
2. Alarms
Alarms are blocking the instrument.
They are displayed on the Alarm tab of the System Warnings menu.
The Alarm tab is re-set at each start. To access the previous alarms, press CTRL + F8.
When an alarm is triggered, the instrument is stopped and turns to "Emergency Stop" status.
If an alarm appears, follow the instructions given in the table on the following pages.
7 - 39
Error messages
Level Code Message Error type Action
ISE module reagent/fluidic error. LB sensor still
7 - 40
detects Standard 1 flow after the aspiration Check the ISE Standard 1 bottle, hydraulic circuit.
ISE low solution inlet excess on
Warning 325 specified time. The LB sensor measurement is Check the valve V4 and readjust the LB sensor.
timeout (error code 24)
ISE module
7 - 41
Error messages
ISE module
Procedures
3. Procedures
Maintenance and adjustments required for the ISE module are divided into procedures
according to the concerned assemblies. This should make any update easier as all
interventions can be done with the corresponding procedure on its own.
The table below lists the ISE maintenance procedures and their frequencies.
For more detailed information, please refer to the instrument user manual.
Maintenance Frequency
ISE module etching Daily if more than 20 samples are run daily
ISE module cleaning Weekly
ISE reagents replacement As needed
Electrodes replacement As needed
An ISE maintenance check up summary is provided in this manual (see on next page) to ensure the
maintenance follow-up. This document can be used as reference to create a maintenance schedule for
customer archives.
6 month Yearly
maintenance maintenance
Rinsing with distilled water and draining.
Rinsing and
See RAS388: ISE module maintenance, 3.1. Rinsing with X
draining
distilled water and draining, page 4.
ISE mix cup cleaning with bleach and rinsing with distilled
water. See RAS388: ISE module maintenance, 3.6. ISE X X
mix cup cleaning, page 10.
Mix cup
Tubing "air sensor to ISE mix cup" replacement.
See RAS388: ISE module maintenance, 3.7. Tubing "air X X
sensor to ISE mix cup" replacement, page 11.
This document can be used as reference to create a maintenance schedule for customer
archives.
RAS441E
Concerns
ISE module physical installation
ISE module startup
Required tools
Hexagonal keys
Phillips screwdriver
Required products
Distilled water
Intervention time
1 h 00
Frequency
On request
1.1. Unpacking
Unpack the ISE module carefully and make sure that all the parts from the package list are present.
Package list
■ Switch the instrument off and disconnect the power supply cable.
■ Open the arms main cover and the ISE cover.
■ Remove the ISE plate and the mother board cover. See RAS377: Covers dismantling, page 1.
J3
■ Guide the cable down to the passage designed for the wires (follow the black "Barcode Reader" wire)
to achieve the correct position.
■ Put the mother board cover back in position.
Tygon tubing
Tygon tubing
Straight fitting
Crystal tubing
A B
■ Connect the power supply cable and switch the instrument on.
For the reference electrode, remove the protection from one side of the electrode and
disconnect the tubing between the two connectors.
For all electrodes, make sure that the O-ring is well-positioned on one side of the electrode
and make sure that the electrode is clean.
O-ring
■ Install the electrodes (after removing the foam supporting the air detector):
Chlore (Cl)
Reference
■ Connect the tubing from LV3- inlet 1 to the upper inlet of the Reference electrode.
■ Connect the tubing from LV4- inlet 1 to the lower inlet of the Reference electrode.
■ Close and fasten the ISE door.
■ Install the Standard 1, the Standard 2 and the Reference solutions.
LV4 LV3
Standard 1
Standard 2
Reference
This diagram is available in the form of a sticker to be stuck on the inside of the ISE cover:
STICKER, ISE HYDRAULIC HAX0271 (1207230271).
To minimize environmental interferences, the ISE module cover must always be closed during
ISE module operation.
A C
Follow the "ISE module check up after intervention" procedure. See RAS537: ISE module check up after
intervention, page 1.
To know the slope and offset range, see Section 7: ISE module, 1.7.2. NA, K, CL normal range,
page 7-37.
Concerns
6 month maintenance
Yearly maintenance
Procedures
Rinsing with distilled water and draining
Syringes O-rings replacement and greasing
Syringes pistons and O-rings replacement
Electrovalve no. 4 cleaning
Tubing "reference electrode to electrovalve no. 4"
replacement
ISE mix cup cleaning
Tubing "air sensor to ISE mix cup" replacement
All tubings and fittings replacement
Isolator and ISE waste tubing replacement
ISE mix cup adjustment
Required tools
Hexagonal keys
Phillips screwdriver
Required products
Distilled water
Bleach
Intervention time
1 h 00
Frequency
On request
1. 6 month maintenance
Here are listed and organized the tasks to be performed during the ISE 6 month maintenance. For each
task, the steps to follow are detailed in chapter 3.
2. Yearly maintenance
Here are listed and organized the tasks to be performed during the ISE yearly maintenance. For each
task, the steps to follow are detailed in chapter 3.
3. Procedures
In order not to damage the pistons, it is advisable to drain the syringes, then rinse them as
quickly as possible to avoid the crystallization of reagents.
■ Go to Services > Customer Services > ISE and press Change electrode.
To avoid risk of instability or impossibility to calibrate, be very careful not to inverse the
pistons when reassembling the syringe.
■ Reinstall the syringe body on the ISE syringes assy without tightening the screws.
■ Perform the same operation with the second syringe.
■ Go to Services > Customer Services > ISE and press Change electrode.
To avoid risk of instability or impossibility to calibrate, be very careful not to inverse the
pistons when reassembling the syringe.
■ Reinstall the syringe body on the ISE syringes assy without tightening the screws.
■ Perform the same operation with the second syringe.
■ Replace the tubing from the lower inlet of the reference electrode to the electrovalve no. 4, inlet 1 (cut
0.170 m of the 0.76 mm Tygon tubing). See ISE module hydraulic diagram, page 13.
■ Remove the ISE cup cover. See RAS377: Covers dismantling, 9. Reagent plate, page 6.
■ Disconnect the 4 tubings from the ISE mix cup.
■ Remove the ISE mix cup.
■ Clean it with bleach (diluted 1/10) and rinse it with distilled water.
■ Replace the tubing from the air sensor inlet to the electrovalve no. 5 (cut 0.085 m of the 0.76 mm Tygon
tubing) and the tubing from the electrovalve no. 5 to the lower inlet of the ISE mix cup (cut 0.103 m of
the 0.76 mm Tygon tubing). See ISE module hydraulic diagram, page 13.
■ Reconnect the 3 other tubings on the ISE mix cup.
■ Put the ISE mix cup back.
■ Put the ISE cup cover back.
Replace all the ISE module tubings and fittings by following the hydraulic diagram. See ISE module
hydraulic diagram, page 13.
To LV4 valve
To waste
■ Cut 750 mm of crystal tubing 4x6 and replace the ISE waste tubing located inside the instrument
between the straight fitting 3.1/2.3 of the ISE module (E1) and the internal central luer connector.
E1
luer connector
luer connector
Perform an ISE mix cup adjustment (see RAS441: ISE module installation, 1.4.1. ISE mix cup
adjustment, page 7).
This diagram is available in the form of a sticker to be stuck on the inside of the ISE cover:
STICKER, ISE HYDRAULIC HAX0271 (1207230271).
Concerns
Check up on serum mode
Preliminary operations
Calibration
ISE activation
Control
Check results
Check up on urine mode
Results validation configuration
Procedure
Required tools
None
Required products
Distilled water
Intervention time
0 h 30
Frequency
On request
The "ISE module check up after intervention" procedure should be performed after an
intervention to verify that the ISE module is functioning properly.
To minimize environmental interferences, the ISE module cover must always be closed during
ISE module operation.
It is necessary to write down the customer configuration to reconfigure the control results
validation, with the customer configuration, at the end of the procedure.
A C
■ Refer to the N Control and the P Control vials to specify the control characteristics. To use
the same configuration later, enter a longer expiration date.
■ Refer to the N Control and the P Control vials to specify the Target value, Min. value and
Max. value for the tests Cl, K and Na.
■ Fill one sample tube with 2 mL of N Control and another one with 2 mL of P Control.
■ Physically position the N Control and the P Control on the programmed rack positions.
■ Then, load the rack on the sample tray.
1.2. Calibration
This part of the procedure has to be done only after the first installation of the ISE module or
after the installation of new electrodes.
■ From the main menu, press the ISE Module Status button.
■ Calculate the difference between the low and high values for each result.
For the three last calibrations, the gap between the calculated differences must be 0.2 mV maximum.
For this example:
- 7.3
- 7.3
- 7.2
The gap is 0.1 mV.
It might be possible, during the first hour after the electrode installation, that the gap exceeds
0.2 mV.
It is due to the electrode stabilization.
In this case, wait for one hour before repeating this part of the procedure.
1.4. Control
■ Go to Worklist > Control and refer to your user manual to create the control request (10 replicates) for
the tests Cl, K and Na on serum.
The 10 replicates for the tests Cl, K and Na on the N Control and the P Control will be performed.
Once the instrument is Ready, check results of the tests Cl, K and Na.
C
■ Select the N Control using the Control
scrolling list (A).
■ Inthe Session Mean area, drag the slider
(B) to display the CV (C).
B
Test CV Max.
CL_S 1.0
K_S 1.0
NA_S 1.0
If you have to run the 10 replicates again, ask for a New Worklist from the Start up window
(use the Change User option from the Shutdown window) so that only the 10 new replicates
are taken into account in the CV calculation.
2.2. Procedure
Please refer to the Standard 2 bottle to specify the control characteristics (name, lot,
expiration date) and to the following table to specify the Target value, Min. value and Max.
value for the tests "CL_U", "K_U" and "NA_U".
Target values
Test Target value Min. value Max. value
CL_U 150 143 157
K_U 7 6.7 7.3
NA_U 200 187.8 212.2
■ Fill one sample cup with 500 µL of Standard 2 and physically position this sample cup on the
programmed rack position.
■ Then, load the rack on the sample tray.
2.2.3. Control
■ Go to Worklist > Control and refer to your user manual to create the control request (5 replicates) for
the tests Cl, K and Na on urine.
The 5 replicates for the tests Cl, K and Na on the Standard 2 will be performed.
■ Perform this operation twice.
Test CV Max.
CL_U 2.0
K_U 1.5
NA_U 2.0
If you have to run the 10 replicates again, ask for a New Worklist from the Start up window
(use the Change User option from the Shutdown window) so that only the 10 new replicates
are taken into account in the CV calculation.
Concerns
ISE module dismantling
ISE module spare parts replacement
Boards replacement
ISE valves replacement
ISE syringes and motors replacement
ISE module mechanical adjustments
ISE mix cup adjustment
Sample arm "ISE Sample" position adjustment
LB sensor adjustment
Required tools
Hexagonal keys
Phillips screwdriver
Voltmeter
Syringe
KIT, ANTISTATIC KIT MZZ015A (1207921015)
Required products
Distilled water
Intervention time
N/A
Frequency
On request
■ Switch the instrument off and disconnect the power supply cable.
A B
Now, it is possible to move the ISE module, but if necessary, remove the power supply cover, the
external and internal sample covers. See RAS377: Covers dismantling, page 1.
At the end of each replacement, proceed to a mechanical adjustment (see 3. ISE module
mechanical adjustments, page 20), run a Global Initialization cycle in Services >
Diagnostics > ISE and follow the "ISE module check up after intervention" procedure (see
RAS537: ISE module check up after intervention, page 1).
■ Switch the instrument off and disconnect the power supply cable.
■ Open the arms main cover and the ISE cover.
■ Dismantle the ISE module until you have access to its connections (See 1. ISE module dismantling,
page 2).
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
CPU-03N
CPU-07N
■ Carefully disconnect:
- the "preampli to main board ISE" cable (A)
- the valves cable (B) A
- the 2 syringe home sensor cables: one of
them from the ISE syringe motor 1/75 (C) B
and the other one from the ISE syringe
motor 1/150 (D) C
- the 2 syringe motor cables: one of them E
D
from the ISE syringe motor 1/75 (E) and the F
other one from the ISE syringe motor 1/150
(F)
■ Remove the ISE software board. See 2.1.1. ISE software board, page 5.
B
■ Disconnect the "preampli to main board
ISE" cable (A) from the ISE preampli board.
■ Unscrew the screw supporting the ground
wire (B).
■ Remove the preampli board assy.
■ Reassemble in reverse order. To reconnect all the tubings correctly: see ISE module hydraulic
diagram, page 18.
■ Reassemble in reverse order. To reconnect all the tubings correctly: see ISE module hydraulic
diagram, page 18.
■ Run a Valve Check cycle in Services > Diagnostics > ISE.
■ Reassemble in reverse order. To reconnect all the tubings correctly: see ISE module hydraulic
diagram, page 18.
■ Run a Valve Check cycle in Services > Diagnostics > ISE.
■ Reassemble in reverse order. To reconnect all the tubings correctly: see ISE module hydraulic
diagram, page 18.
■ Reassemble in reverse order. To reconnect all the tubings correctly: see ISE module hydraulic
diagram, page 18.
■ Cut
the Ty-Raps™ maintaining the syringe
home sensor and syringe motor cables.
■ Reassemble in reverse order. To reconnect all the tubings correctly: see ISE module hydraulic
diagram, page 18.
■ Runa Needle 1 Liquid Aspiration cycle and a Needle 2 Liquid Aspiration cycle in Services >
Diagnostics > ISE.
■ To reconnect all the tubings correctly: see ISE module hydraulic diagram, page 18.
■ Runa Needle 1 Liquid Aspiration cycle and a Needle 2 Liquid Aspiration cycle in Services >
Diagnostics > ISE.
■ Cut
the Ty-Raps™ maintaining the syringe
home sensor and syringe motor cables.
spring spring
■ Reassemble in reverse order.
■ Runa Needle 1 Liquid Aspiration cycle and a Needle 2 Liquid Aspiration cycle in Services >
Diagnostics > ISE.
This diagram is available in the form of a sticker to be stuck on the inside of the ISE cover:
STICKER, ISE HYDRAULIC HAX0271 (1207230271).
■ Connect the power supply cable and switch the instrument on.
Follow the ISE mix cup adjustment procedure (see RAS441: ISE module installation, 1.4.1. ISE mix cup
adjustment, page 7).
Adjust the sample arm in the ISE mix cup by following the sample arm adjustment procedure.
- ISE Sample (rotation) to center the sample needle in the ISE mix cup. See RAS385: Arms, 6.3.5. ISE
Position, page 42.
- Low Position in ISE Tower (vertical) to adjust the sample needle height in the ISE mix cup. See
RAS385: Arms, 6.4.5. "Low Position in ISE Tower", page 53.
4. LB sensor adjustment
■ Remove the ISE V2 mix cup valve assy (See 2.1.3. ISE preampli board assy, page 7).
■ Slowly pull the ISE preampli board assy. The connectors and tubings must stay connected.
TP3
■ Remove the ISE cup cover (See RAS377: Covers dismantling, 9. Reagent plate, page 6).
■ Remove the ISE mix cup.
■ Disconnect the tubing from the ISE mix cup to the air sensor.
■ Check if the adjustment with air in the sensor is still correct. If not readjust it.
■ Check and readjust until both adjustments are correct.
■ When the adjustment is correct, tighten the screws.
Concerns
Introduction
Connection of the ISE module with the laptop
Reminder on the different ISE module status
Communication between instrument and ISE module
Command access in the Dummy PENTRA software
Command validity according to the ISE module status
Dummy PENTRA software use
Command sequence to complete the diagnostic
Explanation of the main error messages
End of operation
Required tools
Hexagonal keys
Phillips screwdriver
Required products
Distilled water
Intervention time
N/A
Frequency
On request
1. Introduction
The Dummy PENTRA software makes the breakdown diagnostic relative to the ISE module easier.
According to the result of the performed tests, the failure can be attributed to the ISE module in itself or
to the instrument.
■ Switch the instrument off and disconnect the power supply cable.
■ Open the arms main cover and the ISE cover.
ISE module
mother board
■ Connect the cable, ref. DAC028A
(1201891028), to the ISE module (in CN2
position) and to the laptop.
Connector
CN2 +
Null modem cable
2.2. Second case (if no cable at your disposal): use of the ISE/
instrument null modem cable
■ Dismantle the ISE module until you have access to its connections (see RAS538: ISE module spare
part replacement, 1. ISE module dismantling, page 2).
■ Remove the mixer cover. See RAS377: Covers dismantling, 15. Mixer cover, page 9.
■ Remove the mother board cover. See RAS377: Covers dismantling, 16. Mother board cover, page 10.
■ Slowly guide the null modem cable down to the passage designed for the wires (follow the black
"Barcode Reader" wire) to reach the ISE module back.
■ Connect the cable to the laptop.
The ISE module exists in seven different statuses. While the instrument is running, the status of the ISE
module is displayed in the ISE tab. Go to Services > Customer Services > ISE.
The status from 0 to 6 of the ISE module are described in the following table:
Code Description
0 Module not initialized
1 Module initialized
2 Module configured
3 Mechanical part initialized
4 Module sleeping
5 Fluidic part initialized
6 Module calibrated
In correct working order, the ISE module evolves sequentially from status 0 to 6, thus from the instrument
start up (Power ON) to the calibrated module achievement, ready for the analyses.
Power ON
This status doesn’t require any
command from the analyzer
Status 0
■ Connect the power supply cable and switch the instrument on.
■ Open the Dummy PENTRA software by double-clicking.
If a USB/series adapter is used, configure under Windows the selected USB port in COM1.
B
A
Some numbers are missing from the sequence. They correspond to commands carried out
by the instrument, but which have no sense to exist in this test software (example of unlisted
command: 100- "Emergency stop").
The commands present in this software are either valid or not according to the ISE module status.
The table below is a summary of the accessible commands (number and designation) according to the
ISE module status:
The Dummy PENTRA software put together all the actions in relation with the ISE module, accessible in
the Customer Services menu and in the Diagnostics menu.
The Dummy PENTRA software V1.32 is compatible with both ABX Pentra 400 and Pentra
C400.
2 1
In the case of a breakdown diagnostic, one or several commands can be selected successively.
■ Double-clickthe command to select it.
A message is displayed. It allows you:
■ If you click OK, the selected command is displayed in part 2 (A) of the window:
■ To cancel a pre-selected command, click the command in part 2 and cancel it (with delete keyboard
key).
■ Enter the number of times the command(s) will be launched in the Repeat times field (B).
By default, the command will be carried out only once.
■ To launch the command without a limit notion: select the Infinity times check box (C).
D
E
B
C
■ When the command is launched, a message is displayed, informing that the selected command is
running.
The command can be stopped by clicking on the STOP button:
* Data can be displayed in these three columns while no analysis have been ordered.
Example: without any value in memory, the following default values will be displayed:
NA K Cl
999.9 999.9 999.9
** The table below summarizes the relation between the indicated value and the selected electrode(s):
Na+ K+ Cl-
0 - - -
1 Yes - -
2 - Yes -
3 Yes Yes -
4 - - Yes
5 Yes - Yes
6 Yes Yes
7 Yes Yes Yes
The command 052 "Set system configuration" allows you to set the use of one, two or three
electrodes according to the binary weight (0=none and 7=all) assigned to the field "Config 1".
To check the change of configuration, launch the command 003.
8.1. Communication test between the ISE module and the laptop
■ If there is a problem during the calibration, an error 03 appears and the system stays in
status 5.
■ If there is no value in memory, the value 999.9 is displayed for each physically present
electrode.
■ All these sequences can be connected to reach directly the status 6 by using the command
051 "Global initialization".
D
E
To perform a measurement command, 50 µL of sample must be poured into the ISE mix cup right before
launching the command.
■ Command 057: "Measure serum"
The figure below is an example of repeatability performed with the Standard 1 which allows you to
compare directly the obtained values with the reference values on Cl, K and Na.
■ ERROR 02: communication problem between the ISE module and the instrument.
Reset the Dummy PENTRA software and switch the ISE module off and on.
■ ERROR 06: command not available in view of the ISE module status.
■ When the diagnostic is done, switch the Dummy PENTRA software off.
■ Switch the instrument off and disconnect the power supply cable.
■ Disconnect your laptop from the ISE module.
■ Reconnect the null modem cable.
■ Reassemble the ISE module in reverse order.
■ Connect the power supply cable and switch the instrument on.
■ Perform the "ISE module check up after intervention" procedure. See RAS537: ISE module check up
after intervention, page 1.
Concerns
ISE module preparation
ISE software version loading
End of operation
Required tools
Hexagonal keys
Phillips screwdriver
Flat screwdriver
Required products
None
Intervention time
1 h 00
Frequency
On request
■ Install
the instrument software version corresponding to the ISE software version you need. See
RAS517: Software version installation, page 1.
■ Switch the instrument off and disconnect the power supply cable.
CPU-03N
(for ABX Pentra 400
only)
Rotary selector
■ If
your ISE module is equipped with the ISE
software board CPU-03N, use a flat
screwdriver to turn the rotary selector from
0 to F (located on the ISE software board).
Position F
Position 0
CPU-07N
(for Pentra C400 only)
SW1 switch
■ If
your ISE module is equipped with the ISE
software board CPU-07N, use a flat
screwdriver to change the SW1 switch
position from E to W (located on the ISE
mother board).
Position W
J5
If needed, use the CABLE, PC/RS L=1000 5-09 P80, ref. DAD124A (1201921124) to simplify
the connection between the RS232 cable and the ISE module.
■ Connect the power supply cable and switch the instrument on.
The following procedure is a generic procedure for the installation of ISE software versions.
The version numbers mentioned are shown as an example only.
The ISE software version installation procedure lightly differs depending on the ISE software
board you have on your ISE module: CPU-03N or CPU-07N.
Make sure to install the ISE software version compatible with your ISE software board.
2.1. ISE software board CPU-03N (for ABX Pentra 400 only)
■ From
the IPL Loader window, press
RomWrite.
■ Press Start.
3. End of operation
■ From the Windows Explorer, go to C:\Program Files and rename the P400 Software folder so that at
the next instrument start, the instrument software is launched.
■ Press the Windows Start button, press Shutdown and then Shutdown.
■ When getting the message "It is now safe to turn off your computer", switch the instrument off and
disconnect the power supply cable.
■ If your ISE module is equipped with the ISE software board CPU-03N, use a flat screwdriver to turn
the rotary selector from F to 0 (located on the ISE software board).
Position F
Position 0
■ If your ISE module is equipped with the ISE software board CPU-07N, use a flat screwdriver to change
the SW1 switch position from W to E (located on the ISE mother board).
Position E
■ Unplug the RS232 cable from the ISE module and plug it into the instrument mother board (J5). Then,
plug the null modem cable into the ISE module.
■ Reassemble the ISE module in reverse order.
■ Connect the power supply cable and switch the instrument on.
■ Enable the ISE module by selecting the Activate ISE Module check box in Services > System
Configuration > Analyser.
■ Run a Global Initialization cycle in Services > Customer Services > ISE.
3. Sample tray.................................................................................................... 8 - 7
6. Cuvette changer.......................................................................................... 8 - 11
19. Covering..................................................................................................... 8 - 32
1. Reagent tray
2
2
8
5
6 9
10
11
7
12
13
14
15
16
2
8
3 9
10
4
11
5
12
13
14
15
6
3. Sample tray
3
9
4. Optical bench
1 6
7
3 8
4 9
10
* For the ABX Pentra 400, the acquisition board ref. XAA483CS (1209109483) and the
spectrophotometer ref. XDA854D (1209134854) are compatible only if the instrument is
equipped with the software version V5.0.6 or higher.
The spectrophotometer ref. XDA854D (1209134854) is delivered with the acquisition board
cable ref. DAD134C (1201923134). This cable is not compatible with the ABX Pentra 400 V1,
the acquisition board cable ref. DAD134B (1201922134) must be used instead.
5. Reaction tray
12
11
13
14
15
16
6
2
4 17
5 18
19
7 24
20
8 21
9
22
10 23
6. Cuvette changer
1
8
3 2
4 9
5
10
11
2
9
3
4
5
6 1
7
10
If the cuvette changer ABX Pentra 400 V1 needs to be replaced, order the cuvette changer
update kit ref. XEC033AS (1209179033). See Cuvette changer update kit, page 8-14.
1 5
2 6
1
2 9
4
6
10. Ventilation
The FAN, MAIN FAN 24 V P60/P80 ref. XBA393A (1209111393) is located at the rear of the
instrument, right below the mother board.
2
3
4
7
4 6
* The part number XBA540C (1209113540) is obsolete and replaced by the kit ASSY,
REAGENT ARM ASSY W/O JIB ref. XDA861CS (1209139861).
1
4
7
3
To position the teflon tubing of the sample needle in the correct way on the mother board
cover, use the CLIPS, PLASTIC D=6.4 MM ref. DBJ025A (1202131025).
5
2
3 6
To position the teflon tubing of the reagent needle in the correct way on the mother board
cover, use the CLIPS, PLASTIC D=6.4 MM ref. DBJ025A (1202131025).
2 1 3
For the ABX Pentra 400 V1 and V2: because the up/down reagent arm motor rotation way is
inverted, it is mandatory to replace the reagent arm vertical motor cable by the new one
(provided in the kit XDA861CS (1209139861)).
1 9
2 10
11
3 12
4 13
5
14
6 15
16
7
8
6 7
1 13 14
2
12 16
3
4
17
2
3 14
5
6 9
7 18
4 13
2 13 15
19
8
20
10 21
11
24
23
22
+ EAC015A (x1)
+ EAC015A (x3)
19. Covering
13
1 14
15
3
4 16
17
5
18
6
19
7
8 20
9
21
22
10
23
11
12
26 25 24
27
1 2
3
3
5
4
6
7
8
10
20
11
19
12
18
13
21
17
14
15 16
2
3
4
5
6
8
9
10
1 2 3 4 5
9
6
23. Computer
5
3 6
8
4
3
4
To check the spare parts compatibility with the different computer models in the field, please
refer to RAS392: Internal computer: 3. Computer parts replacement, page 8.
3 3*
1 4
5
11
6
2
12
10
13
The main fuses, ref. DAR048A (1202001048) or DAR049A (1202001049), are located in the
power plug.
■ Before opening the fuse holder, disconnect the cooling unit power plug!
■ Only use fine fuses with a nominal value as specified and with UL approbation!
5
1
4
8
6
The main fuses, ref. DAR047A (1202001047) or DAR033A (1202001033), are located in the
power plug.
■ Before opening the fuse holder, disconnect the cooling unit power plug!
■ Only use fine fuses with a nominal value as specified and with UL approbation!
1. Tools............................................................................................................... 9 - 2
2. Kits ................................................................................................................. 9 - 3
3. Fuses .............................................................................................................. 9 - 3
4. Stickers .......................................................................................................... 9 - 4
5. Other consumables....................................................................................... 9 - 5
Please note that the complete list of spare parts and consumables is available in the TOOL,
CDROM SPARE PARTS CATALOG ref. RAX021 (1208417021).
1. Tools
2. Kits
3. Fuses
4. Stickers
5. Other consumables
1. Physical connection.................................................................................... 10 - 2
7. Connection test......................................................................................... 10 - 16
7.1. Physical test........................................................................................................................... 10 - 16
7.2. Software test.......................................................................................................................... 10 - 17
8. Troubleshooting ........................................................................................ 10 - 27
8.1. List of warnings about the connection .................................................................................. 10 - 27
8.2. Troubleshooting help ............................................................................................................. 10 - 28
1. Physical connection
The instrument and the Host are connected by a RS232 serial connection, using a RS DB9 cable.
The RS serial port of the instrument, located at the rear of the instrument, is a DB9 male connector.
GND
5 5
9 9 A
4 4 n
H 8 8 a
o TXD TXD l
3 3
s y
t 7 7 s
RXD RXD
2 2 e
6 6 r
1 1
First, it is important to define the laboratory working method i.e. to configure the loading mode in
Services > System Configuration > Analyser.
■ Identification mode: select this mode if all sample tubes are identified with barcode labels.
■ Position mode: select this mode if sample tubes with and without barcode labels are used on the
instrument.
Then, the connection is configured on the instrument in Services > System Configuration > Host
connection.
The Query mode is automatically disabled when the instrument operates in Position mode.
The Sending validated samples option is used to manually ask the Host for supplementary tests on
validated patient samples by using the corresponding function in the Work Balance menu or the Patient
Result list.
This part is used to authorize the character "Space" on the left side of the Sample ID field.
■ If the check box is selected, then the character "Space" is allowed on the left side of the Sample ID
field when manually captured from the instrument as when loaded from the Host. On prints, the
character "Space" is indicated by a rectangle.
■ If the check box is deselected, then the character "Space" is not authorized on the left side of the
Sample ID field and is systematically deleted.
This part is used to enable/disable the automatic transmission of patient and/or control results to the
Host.
2.5. Analyser Id
This field is used to enter the identification number of the instrument by the Host.
This part is used to perform some operations regarding the Host connection.
See Host Tools, page 10-17.
3. Connection protocol
The ABX Pentra 400 / Pentra C400 connection protocol is both the language used for the transmission
of data between the instrument and the LIS (Laboratory Information System) and the way the data is
exchanged. For simplification, we will call protocol the way the data is exchanged and format the
language used.
The ASTM (American Society for Testing and Materials) format is the language used for the transmission
of data on the ABX Pentra 400 / Pentra C400.
There are two analyzer operating modes: monodirectional (i.e. unidirectional) and bidirectional. This is
inherent to the protocol.
On the ABX Pentra 400 / Pentra C400, the bidirectional connection is used.
4. ASTM format
The ASTM format was developed several years ago to standardize the connection between analysis
instruments and LIS. In fact, there were as many connection formats as companies providing
instruments. Each company may use a different protocol for each instrument.
The ASTM proposed one standard for the low level exchange protocol (E-1381) and another for the
format used for the transmission of clinical data (E-1394).
For more information, please refer to the document "Output formats ABX Pentra 400 / Pentra
C400" ref. RAA025, intended for IT Services Companies.
At the protocol level, the data exchange is based on the following model:
The characters <CR> (Carriage Return) and <LF> (Line Feed) are usually placed at the end
of frame for a better organization and reading.
These different frames have an identifier that indicates the nature of transmitted data between <STX>
and <ETX>.
Example
<-- <ENQ>
--> <ACK>
<-- <STX>1H|HEADER<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>2P|PATIENT DEMOGRAPHY<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>3O|ORDER<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>4L|TERMINATOR<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <EOT>
CKSM (Checksum): numerical value, calculated according to the transmitted characters, that ensures
the frame integrity.
Example
<-- <ENQ>
--> <ACK>
<-- <STX>1H|HEADER<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>2P|PATIENT DEMOGRAPHY<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>3O|ORDER<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>4R|RESULT<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <STX>5L|TERMINATOR<CR><ETX>CKSM<CR><LF>
--> <ACK>
<-- <EOT>
CKSM (Checksum): numerical value, calculated according to the transmitted characters, that ensures
the frame integrity.
5. Bidirectional connection
A bidirectional communication goes into both directions. This definition does not give any information
about the nature of transmitted data. We only know that the instrument and the LIS can exchange data
between themselves.
Using this connection type, the instrument can receive orders from the Host and then send results to the
Host.
In this case, the sample tubes are programmed on the instrument. The results are then sent to the Host,
and the Host confirms the data receipt (<ACK>, ACKnowledge).
ACK
ACK
ACK
5.3. The instrument asks the Host for data (Query mode)
In this case, the laboratory must use barcodes. Starting the analyses, the instrument reads the barcode
labels of sample tubes (Identification mode) and asks the Host for the associated requests (Query
mode). The Host sends the corresponding requests to the instrument and once the analyses have been
performed, the instrument sends the results to the Host.
This operating mode is best used when several identical instruments are connected to the
LIS, resulting in one worklist per analyzer.
ENQ
ACK
ACK
ACK
ACK
EOT
--> <ENQ>
<-- <ACK>
--> <STX>1H|\^&||||||||||P|E1394-97|20050111111131<CR><ETX>6A<CR><LF>
<-- <ACK>
--> <STX>2Q|1|^2312019||ALL||||||||0<CR><ETX>7C<CR><LF>
<-- <ACK>
--> <STX>3L|1|N<CR><ETX>06<CR><LF
<-- <ACK>
--> <EOT>
ENQ
ACK
ACK
ACK
ACK
ACK
EOT
Example of response with a request previously entered from the Host for the SID 2312019
The Host sends the requests corresponding to the SID 2312019, read on the instrument.
--> from instrument to Host
<-- from Host to instrument
<-- <ENQ>
--> <ACK>
<-- <STX>1H|\^&|||ABX|||||||P|E1394-97|20050111111502<CR><ETX>47<CR><LF>
--> <ACK>
<--
<STX>2P|1||PID001||NAME^FIRSTNAME||19641223|M|||||PRESCRIPTOR||||||||||||LOCATION<CR><ETX>
14<CR><LF>
--> <ACK>
<-- <STX>3C|1|I|PATIENT COMMENT|<CR><ETX>38<CR><LF>
--> <ACK>
<-- <STX>4O|1|2312019||^^^13\^^^12\^^^14\^^^32\^^^34\^^^37\^^^39|||19900522105500||||A||||1
<CR><ETX>4F<CR><LF>
--> <ACK>
<-- <STX>5C|1|I|ORDER COMMENT<CR><ETX>A1<CR><LF>
--> <ACK>
<-- <STX>6L|1|N<CR><ETX>09<CR><LF>
--> <ACK>
<-- <EOT>
Example of response without request previously entered from the Host for the SID 2312019
--> from instrument to Host
<-- from Host to instrument
<-- <ENQ>
--> <ACK>
<-- <STX>1H|\^&|||ABX|||||||P|E1394-97|20050111111502<CR><ETX>47<CR><LF>
--> <ACK>
<-- <STX>2Q|1|^2312019||||||||||X<CR><ETX>AC<CR><LF>
--> <ACK>
<-- <STX>3L|1|N<CR><ETX>06<CR><LF>
--> <ACK>
<-- <EOT>
The reason why information systems have problems accepting the protocol, regardless of the
protocol type used, often lies with the LIS connection driver development. This connection
level requires great attention. As all the fields (identifiers) are not mandatory, the Host first
needs to be asked to give as little information as possible and then to add information by
studying several possible cases depending on the tubes.
For more information, please refer to the document "Output formats ABX Pentra 400 / Pentra
C400" ref. RAA025, intended for IT Services Companies.
ENQ
ACK
ACK
ACK
ACK
ACK
ACK
EOT
--> <ENQ>
<-- <ACK>
--> <STX>1H|\^&|||01|||||||P|E1394-97|20031118162410<CR><ETX>D7<CR><LF>
<-- <ACK>
--> <STX>2P|1||PID12345||LASTNAME^FIRSTNAME||19641223|M<CR><ETX>C4<CR><LF>
<-- <ACK>
--> <STX>3C|1|I|Patient Comment|G<CR><ETX>FF<CR><LF>
<-- <ACK>
--> <STX>4O|1|2312015||||20031118154703|20031117000000||||||||1|Prescriptor|||||||||F||||Location<CR>
<ETX>EE<CR><LF>
<-- <ACK>
--> <STX>5C|1|I|Order Comment|G<CR><ETX>28<CR><LF>
<-- <ACK>
--> <STX>6R|1|^^^1002^RATIO|5.54|2||A||F|||18991230000000<CR><ETX>1D<CR><LF>
<-- <ACK>
--> <STX>7C|1|I|Flag^NORM_RANGEL|I<CR><ETX>69<CR><LF>
<-- <ACK>
--> <STX>0R|2|^^^13^ALB|5.5494|6||H||F|||20031118162203<CR><ETX>7E<CR><LF>
<-- <ACK>
--> <STX>1C|1|I|Flag^NORM_RANGEH|I<CR><ETX>5F<CR><LF>
<-- <ACK>
--> <STX>2R|3|^^^29^IRON1|-0.01262|6||L||F|||20031118162215<CR><ETX>76<CR><LF>
<-- <ACK>
--> <STX>3C|1|I|Flag^NORM_RANGEL|I<CR><ETX>65<CR><LF>
<-- <ACK>
--> <STX>4L|1|N<CR><ETX>07<CR><LF>
<-- <ACK>
--> <EOT>
ENQ
ACK
NACK
ACK
ACK
ACK
ACK
EOT
When a data is received incorrectly, the <NACK> (Not ACKnowledge) response asks the same data to
be transmitted again.
7. Connection test
This document can be used to make sure that the connection on the instrument is well-configured, and
that the instrument receives orders and sends results correctly.
The physical connection (cable) and the LIS configuration are managed by the IT Services
Company.
Required tools
- RS DB9 cable ref. DAC028A (1201891028)
- Laptop with a free COM serial port or a serial/USB adaptor
- WinASTM software
Use your RS DB9 cable and your simulator to test the physical connection (cable).
If the connection works properly with your RS DB9 cable and your simulator (see 7.2.2. Using the
WinASTM software, page 10-20), connect the instrument and your simulator with the customer cable
and test the communication again.
If the communication does not work, ask the IT Services Company to check and replace the customer
cable.
If the communication works, ask the IT Services Company to check the LIS configuration.
Host Tools
Go to Services > System Configuration > Host connection.
■ Reset connection
Press the Reset connection button to reinitialize the connection process (COMSIL).
If the connection process does not work, it is reinitialized after user confirmation.
If the connection process works properly, a message informs the user and the connection
process is not reinitialized.
■ PurgeHost orders
Press the Purge Host orders button to suppress the pending data receipts.
The pending data receipts are suppressed after user confirmation.
■ Test
communication
Press the Test communication button to test the communication with the Host.
Once the test is done, a message is displayed in the Received character field.
Message Description
ACK (ACKnowledge) Correct acknowledgement, positive response to the test.
XXX Incorrect acknowledgement, negative response to the test.
Time Out Response to the test not received on time.
Process NOK The connection process (COMSIL) does not work.
■ Connection Spy
Press the Connection Spy button to visualize the frames of the communication with the Host, and
search for a character string in these frames.
The following screen is then displayed:
This screen opens in Display mode. In this mode, you can only visualize the frames of the
communication with the Host. The screen is refreshed at each new frame, the last frame is displayed
at the bottom of the screen.
Press the Search button to turn to Search mode.
In Search mode, the screen is not refreshed anymore. You can search for a character string in the
displayed frames as follows:
- Type the character string in the Text to Find field (30 characters max.).
- If necessary, select the Case Sensitive and/or Whole Words check boxes.
If the Case Sensitive check box is selected, the search takes into account the use of
uppercase or lowercase.
If the Whole Words check box is selected, the search is done on the complete character
string.
- Choose the search direction (Forward, Backward) by selecting the corresponding radio button.
- Then, launch the search by pressing the Next button.
Press Cancel to turn to Display mode.
The purpose of this procedure is to make sure that a pending data receipt, created in the
Rs_Data folder, is integrated correctly by the instrument software, and so that the connection
on the instrument is well-configured.
■ Save
this file as follows:
Astm161007104845813.rcv
■ Put this file in the Rs_Data folder.
If the connection is well-configured, the order should be integrated correctly by the instrument software
and created in Worklist > Patient.
If not, check the connection configuration on the instrument and make sure that the test corresponding
to the channel #39 (used above) is enabled.
The purpose of this procedure is to make sure that a pending data transmission, created in
the Rs_Data folder, is sent correctly by the instrument software, and so that the connection
on the instrument is well-configured and the communication with the Host works properly.
If the connection is well-configured, the result should be sent correctly by the instrument software (the
file disappears from the Rs_Data folder) and should be received by the Host.
If not, test the physical connection (cable) and ask the IT Services Company to check the LIS
configuration and that the test corresponding to the channel #18 (used above) is enabled.
■ TheRs_Data folder contains temporary files, created during the communication with the Host.
These temporary files are named as follows: AstmddMMyyhhmmsszzz (date, time, three-digit number)
and the following file extensions are possible.
■A file SEND_TO_SIL can appear in the Rs_Data folder, this file lists the status of data
transmissions from instrument to Host in case of "GeneralException" error (for example).
■ During the instrument initialization, the following message can be displayed:
"Transmission not successful, do you want to continue to process queued messages?".
This message means that data transmissions are pending in the Rs_Data folder.
Press Yes to send the pending data transmissions as soon as the communication with the
Host is running.
Press No to suppress the pending data transmissions.
The WinASTM software should be used only for connection tests on HORIBA Medical
instruments.
■ The purpose of this procedure is to simulate the Host, using the WinASTM software on a
laptop, to send an order to the instrument and to receive a result from the instrument.
■ This procedure consists in simulating the transmission of a test T1 order to the instrument
and checking the result receipt once the analysis has been performed.
■ Note down the connection parameters configured on the instrument in Services > System
Configuration > Host connection.
■ Enter these connection parameters on the WinASTM software in Configuration > RS and Sockets
Settings.
■ Enter the channel #600 corresponding to the test T1 in the available field.
■ Create a test T1 order by filling the Patient and Order fields as follows:
2
2
5 5
4. Select the channel #600 corresponding to the test T1 in the Test scrolling list. Note: If the channel
#600 does not appear in the scrolling list, close and reopen the WinASTM software.
5. Do not forget to click Modify Current Patient/Modify Current Order to save the Patient/Order
fields.
For more information about the different fields, please refer to the document "Output formats
ABX Pentra 400 / Pentra C400" ref. RAA025, intended for IT Services Companies.
1 2
■ Once the test T1 order is created from the Database Records tab, click Send Current Patient With
His Orders to send the test T1 order to the instrument.
■ The order should be correctly integrated by the instrument software and created in Worklist > Patient.
If not, check on the instrument: the instrument status, the loading mode configuration and the
connection configuration. Check on the WinASTM software: the status buttons, the connection
configuration and make sure that the test T1 order is correctly created.
■ In Worklist > Patient, open the order and select the rack position of the control solution physically
positioned on the sample tray. Press OK to validate.
Then, press Start to run the analysis.
■ Once the analysis has been performed, check the result receipt on the WinASTM software.
8. Troubleshooting
No order is integrated by the instrument software and created in Worklist > Patient.
When the instrument is used in connected mode, it is mandatory to select the Identification mode even
if the laboratory does not use barcodes.
When the Position mode is selected, no order is integrated by the instrument software and created in
Worklist > Patient whereas the connection on the instrument is well-configured. In this mode, the
instrument can only send results to the Host.
Please refer to the document "Output formats ABX Pentra 400 / Pentra C400" ref. RAA025
for more information about the ASTM fields.
3. Procedures .................................................................................................. 11 - 7
3.1. Procedure list ...........................................................................................................................11 - 7
3.2. Maintenance check up summary .............................................................................................11 - 8
RAS376: Installation
RAS378: 6 month maintenance
RAS379: Yearly maintenance
RAS393: Check up after intervention
RAS377: Covers dismantling
RAS380: Reagent tray
RAS381: Sample tray
RAS382: Reaction tray
RAS548: Fan and heater replacement
RAS383: Optical bench
RAS656: Partial condensing lens cleaning
RAS386: Mixer
RAS385: Arms
RAS384: Cuvette changer
RAS392: Internal computer
RAS390: Power supply replacement
RAS391: Mother board replacement
RAS394: Sensors check and adjustment
RAS387: Syringe block assembly replacement
RAS389: Waste and water pumps replacement
RAS442: Pressure sensors
RAS533: Windows master installation
RAS517: Software version installation
RAS518: Reagent applications installation
RAS542: Printer installation
RAS814: External barcode reader
RAS624: Cooling unit
1. Preventive maintenance
The table below lists the maintenance procedures and their frequencies.
For more detailed information, please refer to your user manual and daily guide.
Maintenance Frequency
Without mixer: Daily
Needles cleaning with Deproteinizer
With mixer: Weekly
Reagent needle cleaning (external part) Monthly
Wash towers cleaning Monthly
Syringe plunger tips replacement Monthly
Precision test Monthly
Cooling unit (CU400) filter cleaning Monthly
Cooling unit (CU401) condenser cleaning Monthly
Glycol level checking Bimonthly
Filter replacement Bimonthly
Syringes replacement As needed
Needles replacement As needed
Mixer paddle replacement As needed
Lamp replacement As needed
Instrument cleaning and decontamination As needed
Applications update As needed
Software update As needed
■ An antistatic ground mat is one of a number of antistatic devices designed to help eliminate static
electricity. This mat has a conductive material embedded within, which collects the static. The mat
would need to be grounded (earthed). This is usually accomplished by plugging it into the grounded
line in an electrical outlet. It is important to discharge at a slow rate, therefore a resistor should be
used in earthing the mat. This ground mat allows you to connect an antistatic wrist strap.
- A wrist strap:
- A crocodile clip:
■ Install
the wrist strap on the first ground
cord and connect the first ground cord to
the second snap of the antistatic mat.
■ Put the bracelet around your wrist.
To ensure a good contact, ensure that the wrist strap is correctly tightened around your wrist.
3. Procedures
■ Maintenance and adjustments required for the instrument are divided into procedures
according to the concerned assemblies. This should make any update easier as all
interventions can be done with the corresponding procedure on its own.
■ For ISE module procedures, please refer to the ISE module specific section (see Section 7:
ISE module, 3. Procedures, page 7-42).
A maintenance check up summary is provided in this manual (see on next page) to ensure the
maintenance follow-up. This document can be used as reference to create a maintenance schedule for
customer archives.
6 month Yearly
maintenance maintenance
- CU401: Condenser cleaning
- CU400: Filter cleaning
X
See RAS378: 6 month maintenance, 4. Cooling unit,
page 3.
Check up after Run a test T1 or P1 (Precision test) x15, CV < 1%. See
X X
intervention RAS393: Check up after intervention, page 1.
This document can be used as reference to create a maintenance schedule for customer
archives.
Specific instructions are given for previous ABX Pentra 400 hardware versions:
■ V1 corresponds to instruments with serial numbers below 2000.
RAS376H
Installation
RAS376: Installation
Concerns
Instrument installation
Cooling unit installation
ISE module preparation
First start of the instrument
ISE
Mechanical alignments check
Priming
Pressure sensors calibration
Reagent applications installation
Racks
Check up
Required tools
Hexagonal keys
Phillips screwdriver
Graduated ruler
Required products
Distilled water
1. Instrument installation
Before unpacking, control the proper handling of the instrument package during
transportation with the help of the shock indicator "Shockwatch" and the tipping indicator
"Tiltwatch".
Please refer to the Service Information Letter RAN357A to know the procedure to follow for
instrument package reception.
1.1. Unpacking
Unpack the instrument carefully, then make sure that all of the parts from the package list are present.
You can print these following tables and tick off the corresponding check box when the part is present.
Package list
1.2. Location
Keep in mind that the instrument weighs approximately 120 kg (265 lb).
To move the instrument, four persons are required.
The lifting handles provided in the installation kit must be used.
The Power switch and Power supply connection should always be accessible. When
positioning the system for operational use, leave the required amount of space for easy
access to these items.
1.3. Installation
Install the instrument lifting handles in their location, make sure that they are correctly
secured, lift the instrument onto the workbench using the four handles.
In order not to damage needles during installation, disable the arms (vertical and rotation
movements), and put them on a sample cup rack over the reagent tray as shown on the
following picture.
■ Lift
the mixer assembly up, then down by
pressing the red button.
1.4. Syringes
Required products:
- Reagent syringe 1000 µL (provided in the accessories box)
- Sample syringe 100 µL (provided in the accessories box)
■ Manually fill and empty several times the syringes using a container of distilled water to ensure that
the barrel is filled with water and no air bubbles are visible in the syringes.
Use the "Luer" connectors, straws and tubings provided in the installation kit and in the accessories box
to connect distilled water and waste.
B C D
A
■ Connect the instrument distilled water (B) and waste (D) tubings.
■ Connect the 6x9 mm PVC tube to the twisted priming tube (evacuation of condensation water (A)).
Guide with the shortest distance from the side of the instrument to the waste detection assy and cut
to the correct length. Connect it to the big connector of the waste detection assy.
■ If the instrument is equipped with the ISE module option, follow the same procedure for the ISE waste
tubing (C), then connect it to the small connector of the waste detection assy.
The evacuation of condensation water is done by gravity, it is very important to make sure
that tubes do not bend or do not go up. Idem for ISE waste tubing.
This tube must be guided between the cooling unit tubings by the "Chiller tubing support".
See 2. Cooling unit installation, page 13.
Place the ISO sticker (provided in the accessories box) on the waste container.
■ Before plugging the cooling unit tubings, install the connectors (provided with the cooling unit) as
follows:
casings
■ The input tubing of the instrument into the output connector of the cooling unit.
■ The output tubing of the instrument into the input connector of the cooling unit.
See picture below:
To instrument
To cooling unit
■ Install the cooling unit drainage tubing (10-15 cm of the tubing previously cut) as follows:
When you close the ventilation grid, take care to arrange the drainage tubing up as shown on
the figure below.
■ Fill the cooling unit with ethylene glycol and distilled water as follows:
- Fill the cooling unit with two liters of ethylene glycol and complete with distilled water up to the high
mark.
Install the cooling unit under the instrument or at the same level but never on a higher
position.
Proper ventilation requires at least 10 cm (4 inches) space in the front and at the rear.
■ If the instrument is not equipped with the ISE module option and you have to install the ISE
module, refer to RAS441: ISE module installation, page 1.
■ If the instrument is already equipped with the ISE module, refer directly to the ISE module
startup procedure. See RAS441: ISE module installation, 2.1. Electrode and reagent
installation, page 9.
If the date format or the time format is changed, the instrument will reboot automatically after
confirmation.
5. ISE
See RAS441: ISE module installation, 2.2. Start and use of ISE option, page 12 in
Section 7: ISE module.
It is advisable to check the sample needle alignment in order not to damage it.
Always move the sample arm to its upper position (vertical home) before moving the reagent
arm.
Always move the sample and reagent arms to their upper positions before moving a tray.
Always move the reagent arm into its wash tower before moving the sample arm.
■ Check the adjustment of the reagent arm positions in the wash tower by following the reagent arm
adjustment procedure:
- Wash Tower Position (rotation): see RAS385: Arms, 5.3.2. Wash Tower Position, page 29
- Low Position in Wash Tower (vertical): see RAS385: Arms, 5.4.2. "Low Position in Wash Tower",
page 32
■ Check the adjustment of the sample arm positions in the wash tower by following the sample arm
adjustment procedure:
- Wash Tower Position (rotation): see RAS385: Arms, 5.3.2. Wash Tower Position, page 29
- Low Position in Wash Tower (vertical): see RAS385: Arms, 5.4.2. "Low Position in Wash Tower",
page 32
7. Priming
■ Manually fill the two wash towers with distilled water to avoid splashes, then put the optic hatch back.
■ Close the arms main cover, then leave the Diagnostics menu (press Back) and press Startup.
The instrument initializes its mechanical components, wait until the end of the initialization.
Perform the pressure sensors calibration by following the pressure sensors procedure.
See RAS442: Pressure sensors, 3.3. To calibrate the pressure sensors, page 7.
Perform a full installation of the reagent applications (included in the reagent application kit).
See RAS518: Reagent applications installation, page 1.
Before installation, ensure that the reagent application version is compatible with the
software version installed on the instrument. Refer to the compatibility table in the technical
note included in the reagent application kit.
To optimize the "software" support of your customers, this Reagent Application media must
be kept close to the instrument.
10. Racks
The instrument racks are identified by means of barcode and numbered labels.
Place these labels on racks as shown on the stickers plate:
■ HAX0166 (1207230166) for sample rack 1-10
■ HAX0170 (1207230170) for sample cup rack 41-50
■ HAX0173 (1207230173) for calibrator sample rack 71-84
■ HAX0174 (1207230174) for control sample rack 85-99
■ HAX0175 (1207230175) for reagent rack 60-69
■ HAX0188 (1207230188) for calibrator reagent rack 01-15
■ HAX0190 (1207230190) for control reagent rack 30-44
To read barcode format "Interleaved 2 of 5 WITHOUT Check Digit", use the following
stickers:
- HAX0273 (1207230273): NCD SAMPLE RACK STICKERS 1-10 (included in the accessories
box)
- HAX0274 (1207230274): NCD SAMPLE RACK STICKERS 11-20
- HAX0277 (1207230277): NCD SAMPLE CUP RACK ST. 41-50 (included in the accessories
box)
- HAX0278 (1207230278): NCD SAMPLE CUP RACK ST. 51-60
- HAX0279 (1207230279): NCD SAMPLE CUP RACK ST. 61-70
- HAX0280 (1207230280): NCD CAL SAMPLE RACK ST. 71-84 (included in the accessories
box)
- HAX0281 (1207230281): NCD CTRL SAMPLE RACK ST. 85-99 (included in the accessories
box)
Go to Services > System Configuration > Local Settings.
Press Edit and deselect the Check Digit option, then press OK.
Reagent and calibrator/control stickers (STICKER, REAGENT RACK P400 HAX0230 (1207230230)) are
also available to identify solutions, calibrators and controls on the reagent racks, calibrator/control
reagent racks and calibrator/control sample racks.
Place these stickers as shown on the examples below:
11. Check up
Follow the "Check up after intervention" procedure. See RAS393: Check up after intervention, page 1.
6 month maintenance
Concerns
To decontaminate the hydraulic system
To replace the filter
To replace the syringes
Cooling unit
ISE module
To check the mechanical adjustments
To check the barcode readers
To check the spectrophotometer
To check the temperature
To check the sample needle throughput
To calibrate the pressure sensors
To clean and defragment the C:\ and D:\ drives
Check up after intervention
Required tools
Flat screwdriver
Phillips screwdriver
Hexagonal keys
Required products
Bleach
Intervention time
2 h 00
Frequency
Every 6 months
1. Prepair a bottle containing half a liter of bleach diluted to 1 part of bleach for 9 parts of distilled water
(1/10).
2. Prepair a bottle containing half a liter of distilled water.
3. Replace the water tank with the diluted bleach bottle then run several Filling up cycles.
4. Remove the straw from the diluted bleach bottle and wrap it in absorbent paper.
5. Run several Priming Cycle to drain the circuit.
6. Dry the straw with absorbent paper.
7. Plunge the straw into the distilled water bottle then run several Priming Cycle.
8. Remove the straw from the distilled water bottle and wrap it in absorbent paper.
9. Run several Priming Cycle to drain the circuit.
10. Dry the straw well.
11. Decontaminate the water tank (see 1.2. To decontaminate the tanks, page 2).
12. Plunge the straw into the water tank filled with distilled water.
1. Prepair 2 liters of bleach diluted to 1 part of bleach for 9 parts of distilled water (1/10).
2. Pour this dilution into the water tank then shake it several times.
3. Throw the dilution out in a waste container then rinse thoroughly with distilled water.
4. Follow the same procedure to decontaminate the waste tank.
1. Prepair bleach diluted to 1 part of bleach for 9 parts of distilled water (1/10).
2. Fill the wash towers with this dilution then wait a few minutes.
3. Run a Draining cycle to drain the wash towers.
4. Fill and drain the wash towers several times with distilled water.
5. Manually clean the wash towers with absorbent paper.
The filter is located on the right-hand side, at the back of the instrument.
Refer to your user manual to replace the filter.
4. Cooling unit
4.1. To clean the cooling unit condenser (for cooling unit CU401)
1. Go to Services > System Configuration > Analyser and deselect the Activate Cold Area option.
2. Switch the cooling unit off and disconnect the power supply cable.
When you close the ventilation grid, take care to arrange the drainage tubing up as shown
below.
6. Connect the power supply cable and switch the cooling unit on.
Wait ten minutes minimum, between switching off and switching on the cooling unit.
7. Go to Services > System Configuration > Analyser and select the Activate Cold Area option.
4.2. To clean the cooling unit filter (for cooling unit CU400)
If you have just replaced the filter, it is not necessary to clean it now.
1. Remove the filter with its metallic support from the cooling unit grid.
2. Remove the filter from its metallic support.
3. Clean the filter with water and let it dry.
4. Once dry, put the filter back in its metallic support.
5. Put the filter with its metallic support back on the cooling unit grid by fitting the two metallic pieces
in the grid holes.
5. ISE module
Refer to the procedure RAS388: ISE module maintenance, 1. 6 month maintenance, page 2 in the
section 7: ISE module.
Always move the reagent arm into its wash tower before moving the sample arm.
Always move the sample arm to its vertical home position before moving the reagent arm.
1. Check the adjustment of all the sample arm positions listed below. Refer to the procedure RAS385:
Arms, 6. Sample arm adjustment, page 36.
- Cuvette: Cuvette Position (rotation) and Low Position in Cuvette (vertical)
- Wash tower: Wash Tower Position (rotation) and Low Position in Wash Tower (vertical)
- Reagent rack (rotation): R1 Pos.-Reagent Rack, R2 Pos.-Reagent Rack, R3 Pos.-Reagent Rack
- Calibrator/control reagent rack (rotation): R1 Pos.-Cal/Ctrl Rack, R2 Pos.-Cal/Ctrl Rack, R3
Pos.-Cal/Ctrl Rack
- Cassette (rotation): R1 on Cassette and R2 on Cassette
- Reagent rack, calibrator/control reagent rack and cassette (vertical): Low Position in Reagent
rack, Low Position CalCs on reagent tray, Low Position in Cassette
- Sample (rotation): External Sample and Internal Sample
- Sample (vertical): Low Position in Sample Cup and Low Position in Sample Tube
- ISE tower: ISE Sample (rotation) and Low Position in ISE Tower (vertical)
2. If necessary, readjust the positions.
1. Check the adjustment of all the reagent arm positions listed below. Refer to the procedure RAS385:
Arms, 5. Reagent arm adjustment, page 23.
- Cuvette: Cuvette Position (rotation) and Low Position in Reaction Tray (vertical)
- Wash tower: Wash Tower Position (rotation) and Low Position in Wash Tower (vertical)
- Reagent rack (rotation): R1 Pos.-Reagent Rack, R2 Pos.-Reagent Rack, R3 Pos.-Reagent Rack
- Cassette (rotation): R1 on Cassette and R2 on Cassette
- Reagent rack and cassette (vertical): Low Position in Reagent/Cal/Ctrl Rack and Low Position
in Cassette
2. If necessary, readjust the positions.
1. Check the adjustment of all the mixer positions listed below. Refer to the procedure RAS386: Mixer,
5. Adjustments, page 17.
- Home position
- Above Reaction Tray position and Cuvette position
2. If necessary, readjust the positions.
1. Refer to the procedure RAS384: Cuvette changer, 4.9. Adjustment check, page 47 to check the
adjustment of the cuvette changer.
2. If necessary, readjust the cuvette changer. See RAS384: Cuvette changer, 4. Adjustments, page 31.
1. Check the adjustment of the reagent barcode reader position. Refer to the procedure RAS380:
Reagent tray, 4.4. Reagent barcode reader position, page 24.
2. If necessary, readjust the position.
3. Check the adjustment of the sample barcode reader position. Refer to the procedure RAS381:
Sample tray, 4.3. Sample barcode reader position, page 17.
4. If necessary, readjust the position.
Refer to the procedure RAS383: Optical bench, 4. Optical bench check, page 31.
4. Make sure that the current temperatures for the following are correct.
- Needle Heating: 37°C +/- 1.5°C
- Reaction Heating: 37°C +/- 0.25°C
- Refrigerated Area: between 4 and 10°C
The lights should be green.
This procedure allows you to check the sample needle and the water pump flow.
A
4. Go to Services > Diagnostics > Tray.
5. Select the Reagent option (A) then press
Motor Off (B).
Refer to the procedure RAS442: Pressure sensors, 3.3. To calibrate the pressure sensors, page 7.
1. Press the Windows Start button and go to Programs > Accessories > System Tools > Disk
Cleanup.
1. Press the Windows Start button and go to Programs > Accessories > System Tools > Disk
Defragmenter.
Right-click the Recycle Bin and then click Empty Recycle Bin.
Yearly maintenance
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
Concerns
Instrument
Reagent tray cleaning
Arms assembly greasing (for ABX Pentra 400 V1 only)
Reaction tray cleaning
Cuvette changer endless screw greasing
Cooling unit
Cooling unit CU401
Cooling unit CU400
ISE module
6 month maintenance procedure
Required tools
Flat screwdriver
Phillips screwdriver
Hexagonal keys
Torx key
Required products
Distilled water
Bleach
Intervention time
3 h 30
Frequency
Yearly
1. Instrument
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the sample tray, the insulating cover and the reagent tray (see RAS380: Reagent tray, page 1)
to access the reagent tray fans.
■ Connect the power supply cable and switch the instrument on.
■ Make sure that the reagent tray fans are working properly.
■ Switch the instrument off and disconnect the power supply cable.
■ Use a brush to remove dust from the reagent tray.
■ Use absorbent paper to clean the reagent tray and the barcode reader window.
It is advisable to remove the needles before dismantling the arms assembly (in order not to damage
them).
■ Use the syringe to grease the arms through the two holes on each arm body.
■ Reassemble in reverse order.
After the arms assembly greasing procedure, it is advisable to check the mechanical adjustments of
the sample and reagent arms. See RAS378: 6 month maintenance, 6. To check the mechanical
adjustments, page 5.
■ Follow the reaction tray dismantling procedure. See RAS382: Reaction tray, page 1.
A
■ Unscrew the 7 CHC screws, disconnect the
flap door (A) switch and unscrew the NTC to
remove the upper case.
■ Remove dust from the reaction tray using a brush and a vacuum cleaner.
■ Clean the crown wheel using a brush and a vacuum cleaner.
■ Clean the roller groove using absorbent paper.
■ Blow dust off the spectrophometer lenses, using an aerosol duster.
■ Reassemble in reverse order.
This procedure does not apply to the ABX Pentra 400 V1.
2. Cooling unit
Follow the procedure corresponding to the cooling unit model you have:
- 2.1. Cooling unit CU401, page 7
- 2.2. Cooling unit CU400, page 9
- Put the glycol sticker on the tank (both provided in the kit).
- Slightly tilt the cooling unit forwards to drain completely the cooling unit.
- Then, screw the bleed screw and remove the drainage tubing from the tank.
When you close the ventilation grid, take care to arrange the drainage tubing up as shown on
the figure below.
■ Fill the cooling unit with ethylene glycol and distilled water as follows:
- Fill the cooling unit with 2 liters of ethylene glycol and complete with distilled water up to the high
mark.
The liquid level (glycol + distilled water) exceeds lightly the middle mark of the window.
3. ISE module
See RAS388: ISE module maintenance, 2. Yearly maintenance, page 3 in Section 7: ISE module.
It is not necessary to perform the cooling unit filter cleaning (for cooling unit CU400 only)
because it has been replaced.
Concerns
Preliminary operations
Calibration
Control
Check results
Required tools
None
Required products
Distilled water
Intervention time
1 h 30
Frequency
On request
The "Check up after intervention" procedure, also called "Precision test" procedure, should
be performed after an intervention to verify that the instrument is functioning properly. This
procedure consists in checking the pipetting precision with the ABX Pentra Qualitest Solution
or the ABX Pentra Precitest Solution.
1. Preliminary operations
■ Go to Calibration/Control > Control and refer to your user manual to configure either the ABX Pentra
Qualitest Solution as a control for the test T1 or the ABX Pentra Precitest Solution as a control for the
test P1.
■ For the test T1, refer to the control solution vial to specify the control characteristics as the
Target Value, Min. Value and Max. Value.
■ For the test P1, specify the control characteristics as follows:
- Target Value: 600 ΔA,
- Min. Value: 500 ΔA,
- Max. Value: 700 ΔA
■ Go to Reagent Configuration > Configuration and refer to your user manual to configure distilled
water as a reagent for the test T1 or P1.
■ Physically position either two vials of distilled water (15 mL and 10 mL) for the test T1 or a 15 mL vial
of distilled water for the test P1 on the programmed rack position.
■ Then, load the rack on the reagent tray.
It is necessary to write down the customer configuration to reconfigure the results validation
of calibrations and controls, with the customer configuration, at the end of procedure.
2. Calibration
■ Go to Worklist > Calibration and refer to your user manual to create the calibration request for the
test T1 or P1.
3. Control
4. Check results
First, make sure that all the results (15 replicates) were validated automatically.
A
C
■ If the test results are bad, see Section 6: Troubleshooting, 2.1.1. Repeatability, page 6-42.
■ If you have to run the 15 replicates again, ask for a New Worklist from the Start up window
(use the Change User option from the Shutdown window) so that only the 15 new
replicates are taken into account in the CV calculation. Use new control solution, use fresh
distilled water on the rack.
Covers dismantling
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
■ V2 corresponds to instruments with serial numbers between 2000 and 2999.
Concerns
Arms main cover and ISE cover
Sample covers
Power supply cover
ISE plate
Optic hatch
Arms covers
Cuvettes tray plate
Reagent cover
Reagent plate
Recuperation jar
Loader cover
Cuvettes hatch
Connection hatch
Cuvettes cover
Mixer cover
Mother board cover
Arm bracket covers
Mixer plate
Required tools
Hexagonal keys
Flat screwdriver
Phillips screwdriver
Required products
None
■ Switch the instrument off and disconnect the power supply cable.
A
B
2. Sample covers
4. ISE plate
■ Ifthe instrument is not equipped with ISE module, follow the procedure below.
■ If the instrument is equipped with ISE module, see RAS538: ISE module spare part
replacement, 1. ISE module dismantling, page 2.
5. Optic hatch
Press
6. Arms covers
8. Reagent cover
9. Reagent plate
■ First,
remove the ISE cup cover by
unscrewing the BHC screw.
■ Then,
unscrew the 5 cruciform screws to
remove the reagent plate.
If the instrument is not equipped with ISE module, you have to remove the ISE plate instead
of the ISE cup cover. See 4. ISE plate, page 3.
Pull
Hold the arms in position when unscrewing in order not to damage the needles.
The arm boards are sensible to electrostatic discharge. In order not to damage those boards,
do not touch them.
Reagent tray
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
Concerns
Reagent tray dismantling
Reagent tray parts replacement
Impacted adjustments
Adjustments
Required tools
Hexagonal keys
Torx key
Open-end wrench
Phillips screwdriver
TOOL, REAG TRAY ADJUSTING TOOL XDB097AS
(1209149097)
TOOL, DUMMY REAGENT NEEDLE GBM1124 (1203601124)
TOOL, DUMMY SAMPLE NEEDLE GBM1125 (1203601125)
Required products
None
Intervention time
N/A
Frequency
On request
The reagent tray dismantling allows you to access the reagent tray parts that can be replaced:
- barcode reader
- rollers
- home sensor
- motor
- fans
- NTC
- reagent tray closing assy
- reagent tray door sensor.
See 2. Reagent tray parts replacement, page 6
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
Open the arms main cover and the ISE cover.
Remove the external and internal sample covers, the power supply cover, the optic hatch, the left arm
cover, the cuvettes tray plate, the reagent cover and the reagent plate.
■ If
the instrument is equipped with ISE module, you have to remove the ISE module. See RAS538: ISE
module spare part replacement, 1. ISE module dismantling, page 2.
■ Remove the barcode reader cover by unscrewing the 2 BHC screws and disconnecting the LED
connector from the sample relay board (J2).
■ Disconnect the fan from the right side of the tray, then remove the insulating cover by unscrewing the
13 Torx screws and the 2 Torx F screws.
When reassembling the reagent tray, put the reagent tray into gear on the tensioner roller first.
Then, pull on the reagent tray to put it into gear on the 2 centering rollers. Never dismantle
the motor or the tensioner roller to put the reagent tray back in place.
■ Followthe reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
barcode reader.
■ Remove the mother board cover. See RAS377: Covers dismantling, page 1.
Marks
It is important to mark the position of the barcode reader support to keep the mechanical
adjustment done in factory.
The position of the barcode reader support is adjusted so that the barcode reader beam
passes crosswise through a sector of the reagent tray. The angle formed from one reagent
tray sector extremity to the other is 12°.
12°
■ Unplug the barcode reader connector from the mother board (J4), then remove the barcode reader.
■ Follow the reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
rollers.
CHC screws
- Assemble the roller spacer plate on the roller adjusting support by screwing the 2 CHC screws M3x6
in the tappings # 2 and 3.
- Screw the roller adjusting support on the reagent tray by using the 2 CHC screws M4x8.
If you cannot adjust the tensioner roller to have 2.5 mm between the roller support and the L
plate, then reassemble the roller spacer plate on the roller adjusting support by screwing the
2 CHC screws M3x6 in the tappings # 1 and 2.
■ Follow
the reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
home sensor.
■ Remove the reagent tray to put the front deflector back and reassemble in reverse order.
■ Replace the motor, fasten the 3 CHC screws and washers and reconnect the motor connector.
■ Put the reagent tray back to adjust the motor position.
■ Make sure that there is no play between the reagent tray and the motor pinion but do not over-tighten
the motor.
If necessary, adjust the motor position by unscrewing the 3 CHC screws and washers.
■ Reassemble in reverse order.
Peelable spacer
■ Disconnectthe motor connector and
remove the motor with its peelable spacer.
■ Replace the motor with the old peelable spacer, fasten the 3 CHC screws and washers and reconnect
the motor connector.
The peelable spacer is used to adjust the motor height positioning. This adjustment is done
by the factory. You have to replace the motor with the old peelable spacer to keep the
adjustment done by the factory.
■ Put the reagent tray back to adjust the motor position.
■ Make sure that there is no play between the reagent tray and the motor pinion but do not over-tighten
the motor.
If necessary, adjust the motor position by unscrewing the 3 CHC screws and washers.
■ Reassemble in reverse order.
■ Follow the reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
fans.
■ Pull the fan up to remove it from the tray and cut the Ty-Raps™ to release the fan and its wires.
■ Disconnect the fan connector.
■ Unscrew the 2 CHC screws to release the fan from its support.
■ Replace the fan and reassemble in reverse order.
■ Caution! Put the fan back on the tray by pressing carefully on the two sides of the fan in
order not to break the fan.
■ Ensure that the fan is positioned in the correct direction: the letterings must be placed
towards the tray center.
Press both sides
Letterings
■ Follow the reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
NTC.
■ Followthe reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
reagent tray closing assy.
Connectors SW1
■ Replace the reagent tray closing assy and reassemble in reverse order.
■ Followthe reagent tray dismantling procedure (see 1. Reagent tray dismantling, page 2) to access the
reagent tray door sensor.
■ Disconnect the sensor connector.
■ Unscrew the black nut to release the sensor.
■ Replace the sensor as well as its washer and nut and reassemble in reverse order.
Make sure that there is a space of 1 to 3 mm between the sensor and the upper side of the
tray.
1-3 mm
Black nut
3. Impacted adjustments
4. Adjustments
If the cassette, reagent rack or calibrator/control reagent rack position adjustments are
modified, then the corresponding reagent arm and sample arm position adjustments will
have to be checked and readjusted if necessary. See RAS385: Arms, page 1.
The following table lists the functional positions to adjust. Those positions are reached by three different
types of adjustment:
- the combination of two movements to obtain a centering or
- performing an automatic "AUTO" adjustment or
- performing a manual "MAN" adjustment
The table also indicates the tool required to perform those adjustments.
Modules
Reagent Tray
Sector Position Target Type Tool
Sample arm rotation
Sector 1 Cassette
R1 on cassette 1 R1 Pos.-Cassette for Sample Arm
R2 on cassette 2 R2 Pos.-Cassette for Sample Arm
Sector 2 Reagent rack
R1 Pos.-Reagent Rack 1-A R1 Pos.-Reagent Rack for Sample Arm
R2 Pos.-Reagent Rack 2-A R2 Pos.-Reagent Rack for Sample Arm
R3 Pos.-Reagent Rack 3-A R3 Pos.-Reagent Rack for Sample Arm
Sector 3 Cal/Ctrl rack
R1 Pos.-Cal/Ctrl Rack 1 R1 Pos.-Cal/Ctrl Rack for Sample Arm
R2 Pos.-Cal/Ctrl Rack 2 R2 Pos.-Cal/Ctrl Rack for Sample Arm
R3 Pos.-Cal/Ctrl Rack 3 R3 Pos.-Cal/Ctrl Rack for Sample Arm
Modules
Reagent Tray
Sector Position Target Type Tool
Reagent arm rotation
Sector 1 Cassette
R1 on cassette 1 R1 Pos.-Cassette for Reagent Arm
R2 on cassette 2 R2 Pos.-Cassette for Reagent Arm
Sector 2 Reagent rack
R1 Pos.-Reagent Rack 1-A R1 Pos.-Reagent Rack for Reagent Arm
R2 Pos.-Reagent Rack 2-A R2 Pos.-Reagent Rack for Reagent Arm
R3 Pos.-Reagent Rack 3-A R3 Pos.-Reagent Rack for Reagent Arm
Sector 3 Cal/Ctrl rack
R1 Pos.-Cal/Ctrl Rack* 1 R1 Pos. Cal/Ctrl Rack for Reagent Arm*
R2 Pos.-Cal/Ctrl Rack* 2 R2 Pos. Cal/Ctrl Rack for Reagent Arm*
R3 Pos.-Cal/Ctrl Rack* 3 R3 Pos. Cal/Ctrl Rack for Reagent Arm*
Reagent Barcode
Reader
Sector 36 Cassette
1 Central Loading Reagent Position MAN
* At the moment, these functional positions are not used on HORIBA Medical range.
The "Reag tray adjusting tool" represents the functional positions to adjust as follows:
- C1 and C2: functional positions of a cassette.
- R1, R2 and R3: functional positions of a reagent rack, positions A1, A2 and A3.
- CS1, CS2 and CS3: functional positions of a Cal/Ctrl rack.
■ Connect the power supply cable and switch the instrument on.
Ensure that the reagent and sample arms are in their respective wash towers.
A
■ Put different cassettes and racks on the
reagent tray.
■ Go to Services > Diagnostics > Barcode
Test.
■ Select the Reagent radio button (A).
■ Then, press Check Tray (B).
At the end of the cycle, make sure that the
position of cassettes and racks on the B
screen corresponds to the position on the
reagent tray.
■ In
the Target scrolling list, select Central
Loading Reagent Position (F). G
■ In the Sector scrolling list, select any sector
("7" for this example) (G). F
■ Load the "Reag tray adjusting tool" in the reagent tray. See 4.3. Preliminary procedure, page 23.
■ Replacethe reagent and sample needles respectively by the "Dummy reagent needle" (see RAS385:
Arms, 5.2. "Dummy reagent needle" installation, page 25) and the "Dummy sample needle" (see
RAS385: Arms, 6.2. "Dummy sample needle" installation, page 38).
Adjustment example
Adjustment of a sampling with the reagent needle in a cassette in position "C1".
Aim of this procedure: center the reagent needle in the R1 on Cassette position. This
adjustment is performed with the "Reag tray adjusting tool" and the "Dummy reagent
needle".
R1 on Cassette
R2 on Cassette
■ In
the Target scrolling list, select R1 Pos.-
Cassette for Reagent Arm (F).
■ Press Check Home (C). F
■ Press Check Position to move the cassette
to the R1 Pos.- Cassette for Reagent Arm
position (H), then check the "Reag tray E
adjusting tool" position: C H
■ Adjust the position by changing the number of steps in the Target field for the R1 Pos.- Cassette for
Reagent Arm position (E).
- Y1 - Increase the number of steps to move the tray anticlockwise.
- Y2 - Decrease the number of steps to move the tray clockwise.
Y1 Y2
OK
■ Press Check Home (C) to move the reagent tray to its home position, then check the position again
(press Check Position (H)).
-
+
The principle of the adjustment consists in a combination of two movements: the reagent tray
rotation (a) and the reagent arm rotation (b).
If necessary, repeat the "a" and "b" adjustments by changing each adjustment with the + and
- buttons.
Follow the same adjustment principle for all the functional positions listed in the functional positions
table. See 4.1. Functional positions to adjust, page 20.
Pay attention to select the correct module concerned and to correctly set the sectors, the
positions and the targets.
■ Remove the "Dummy sample needle" and the "Dummy reagent needle" and put the sample and
reagent needles back.
■ Remove the "Reag tray adjusting tool" from the reagent tray.
Sample tray
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
Concerns
Sample tray dismantling
Sample tray parts replacement
Impacted adjustments
Adjustments
Required tools
Hexagonal keys
Torx key
Open-end wrench
Flat screwdriver
Phillips screwdriver
TOOL, DYNAMO. SCREWDRIVER A302 MAG019A
(1207851019)
TOOL, DUMMY SAMPLE NEEDLE GBM1125 (1203601125)
Required products
None
Intervention time
N/A
Frequency
On request
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
Open the arms main cover and the ISE cover.
Remove the external and internal sample covers.
This cover dismantling is enough to be able to adjust the sample tray. See 4. Adjustments,
page 16. But, if necessary, the sample tray can be removed as follows.
■ Remove the barcode reader cover by unscrewing the 2 BHC screws and disconnecting the LED
connector from the sample relay board (J2).
■ The barcode reader frequency (550 Hz) allows the reading of high resolution barcodes
(higher than or equal to 0.16 mm). However, this frequency does not allow the reading of
higher resolution barcodes (lower than 0.16 mm).
■ To know which adjustments have to be performed after parts replacement:
see 3. Impacted adjustments, page 15.
■ Remove the barcode reader cover by unscrewing the 2 BHC screws and disconnecting the LED
connector from the sample relay board (J2).
To position correctly the barcode reader, screw the 2 CHC screws on the barcode reader
support pushing the barcode reader as indicated on the following picture.
■ Remove the barcode reader cover by unscrewing the 2 BHC screws and disconnecting the LED
connector from the sample relay board (J2).
■ Remove the belt from the motor pinion to pass the sample tray home sensor connector through the
opening under the reagent tray.
■ Unscrew the CHC screw to release the sample tray home sensor and its wires.
■ Replace the sample tray home sensor and reassemble in reverse order.
Be very careful when you put back the cover of the computer fan box because you can touch/
disconnect the little board, shown on the following picture, with the cover (depending on the
computer model).
A
B
■ Unscrew the CHC screw to release the sample tray home sensor and its wires.
■ Replace the sample tray home sensor and reassemble in reverse order.
Be very careful when you put back the cover of the computer fan box because you can touch/
disconnect the little board, shown on the following picture, with the cover (depending on the
computer model).
■ To remove the motor from the instrument, it is necessary to slightly lift the reagent tray up as follows:
■ Replace the motor, put the belt back on the motor pinion and fasten the left CHC screw and washer.
■ Put the belt back on the sample tray wheel and fasten the right CHC screw and washer.
■ Tighten the left and right CHC screws.
■ Reassemble in reverse order.
Be very careful when you put back the cover of the computer fan box because you can touch/
disconnect the little board, shown on the following picture, with the cover (depending on the
computer model).
Because the reagent tray has been lifted up, check all the centering positions of the reagent
and sample arms using the "Reag tray adjusting tool", the "Dummy reagent needle" and the
"Dummy sample needle". See RAS385: Arms, page 1.
3. Impacted adjustments
4. Adjustments
When you adjust a position by changing the number of steps for this position, press Check
Home, then check the position again (press Check Position) to validate and save the new
adjustment.
The following table lists the functional positions to adjust. Those positions are reached by the
combination of two movements to obtain a centering .
The table also indicates the tool required to perform those adjustments.
Modules
Sample Tray
Sector Position Target Type Tool
Sample arm rotation
External Sample 1 2 External Sampling Pos.
■ Connect the power supply cable and switch the instrument on.
■ Go to Services > Diagnostics > Tray.
■ Before starting the position adjustments, load a sample cup rack on the sample tray in position "1".
B
■ Select the Sample radio button (A).
■ Inthe Sector and Position scrolling lists,
select "1" and "1" (B).
■ Press Check Home (C).
C
■ To adjust this position, remove the barcode reader cover (see 1. Sample tray dismantling, page 2) to
access the sample relay board.
■ Perform the Preliminary procedure, page 17 but load a sample rack instead of a sample cup rack.
■ In
the Target scrolling list, select Sample
Bar code reader Position (D).
■ Enter
"332" in the Target field for the
Sample Bar code reader Position position D
(F).
■ PressCheck Home (C), then press Check F
Position (E). C E
■ Close the Diagnostics menu and answer OK at the question: "Do you want to save parameters?".
■ Slightly
loosen the 2 CHC screws on the
barcode reader support.
The vertical centering of the beam is no more required (lightly positioned under the window)
because the tube detector position is fixed from now.
■ Perform the Preliminary procedure, page 17 but load a sample rack instead of a sample cup rack.
■ In
the Target scrolling list, select Sample
Tube Detector Position (A).
■ Enter
"3860" in the Target field for the
Sample Tube Detector Position position A
(B).
■ PressCheck Home (C), then press Check B
Position (D). C D
The LED of the sample tube detector is lit (red light (B)) when the reflector is detected and
unlit when the reflector is not detected.
■ Make sure that all types of sample tubes and cups are correctly detected as follows:
- Load 6 sample racks/sample cup racks with several sample tubes and cups on the sample tray.
- Go to Services > Diagnostics > Barcode Test.
■ If some sample tubes and cups are detected on physically empty positions, lightly turn the
potentiometer clockwise and check the detection again (see above).
■ If some sample tubes and cups are not detected, slightly turn the potentiometer anticlockwise and
check the detection again (see above).
The most sensitive positions are the rack positions "1" and "10" for each rack.
Check the detection with and without sample tubes and cups on these positions.
■ Replace the sample needle by the "Dummy sample needle". See RAS385: Arms, 6.2. "Dummy sample
needle" installation, page 38.
Adjustment example
Adjustment of a sampling with the sample needle in a sample cup (or tube) in internal position.
■ To adjust the sample tray position (see Sample position, gray arrows) change the number of steps in
the Target field for the Internal Sampling Pos. position (F).
- Increase the number of steps to move the tray anticlockwise.
- Decrease the number of steps to move the tray clockwise.
Sample position
■ Press Check Home (2) to move the sample arm to its vertical home position.
■ To adjust the sample arm position (see Sample position, blue arrows) change the number of steps in
the Position field for the Internal Sample position (7).
- Increase the number of steps to turn the sample arm clockwise.
- Decrease the number of steps to turn the sample arm anticlockwise.
The principle of the adjustment consists in a combination of two movements: the sample tray
rotation (a) and the sample arm rotation (b).
If necessary, repeat the "a" and "b" adjustments by changing each adjustment with the + and
- buttons.
11
A B
Follow the same adjustment principle for the external position described in the functional positions
table. See 4.1. Functional positions to adjust, page 16.
Pay attention to select the correct module concerned and to correctly set the sectors, the
positions and the targets.
■ Remove the "Dummy sample needle " and put the sample needle back.
■ Put the covers back.
Reaction tray
Concerns
Reaction tray dismantling
Reaction tray parts replacement
Impacted adjustments
Adjustments
Required tools
Hexagonal keys
Hexagonal screwdriver
Flat screwdriver
Phillips screwdriver
OPTICAL, SEGMENT 1XXX TEST 9200787 (1229200787)
TOOL, TEST SEGMENT XDA893A (1209131893)
TOOL, DUMMY REAGENT NEEDLE GBM1124 (1203601124)
TOOL, DUMMY SAMPLE NEEDLE GBM1125 (1203601125)
Required products
None
Intervention time
N/A
Frequency
On request
In order not to damage the needles during dismantling, disable the arms (vertical and rotation
movements) and put them on a sample cup rack over the reagent tray as shown on the
following picture.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the loader cover, the cuvettes hatch, the connection hatch and the cuvettes cover.
- Lift the mixer assembly up by pressing the red button.
- Remove the optic hatch, the left arm cover, the cuvettes tray plate and the mixer plate.
■ Remove the unload rack.
■ Remove the load rack as follows:
- Open the 2 adhesive collars and release the wires of the "rack used segment full" sensor.
- Disconnect the "rack used segment full" sensor (C19) and unscrew the 6 CHC screws.
■ First, follow the reaction tray dismantling procedure. See 1. Reaction tray dismantling, page 2.
■ Install the new flap door switch then fasten the 2 CHC screws.
■ Make sure that the flap door switch works properly by hearing a characteristic "click". If not, adjust it
by unscrewing/screwing the 2 CHC screws.
■ Connect the 2 flap door switch cables.
■ Reinstall the flap door switch cover.
■ Adjust the flap door switch cover with the 2 CHC screws so that the hatch closes properly by
magnetization.
■ Reassemble in reverse order.
■ First, follow the reaction tray dismantling procedure. See 1. Reaction tray dismantling, page 2.
Make sure that the holder disk is correctly positioned to remove the upper case without
damaging the NTC.
NTC
Holder disk
When reinstalling the NTC on the upper case, ensure that only the blue part of the cable is in
the upper case notch.
NTC cable
■ First, follow the reaction tray dismantling procedure. See 1. Reaction tray dismantling, page 2.
■ Unscrew the 7 CHC screws, disconnect the flap door switch and unscrew the NTC to remove the
upper case. See 2.2. NTC replacement, page 5.
■ Replace the motor, fasten the 2 CHC screws and reconnect the motor connector.
■ Make sure that there is no play between the reaction tray crown wheel and the motor pinion but do not
over-tighten the motor. If necessary, adjust the motor position by unscrewing the 2 CHC screws.
■ Reassemble in reverse order.
■ Install the new lateral roller. The screws must be placed alongside the crown wheel.
■ Reassemble in reverse order.
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 2.4.3.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 12.
■ Follow the optical bench dismantling procedure until you removed the optical bench. See RAS383:
Optical bench, 1. Optical bench dismantling, page 2.
Roller axis
0.2 mm
Adhesive tape
■ Leave the adhesive tape on the crown wheel and check the position of the 2 other upper rollers.
■ Remove the adhesive tape.
■ Reassemble in reverse order.
2.4.3.2. Specific procedure ABX Pentra 400 with an old model of optical bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
Roller axis
0.2 mm
Adhesive tape
■ Leave the adhesive tape on the crown wheel and check the position of the 2 other upper rollers.
■ Remove the adhesive tape.
■ Reassemble in reverse order.
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 2.4.4.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 15.
2.4.4.2. Specific procedure ABX Pentra 400 with an old model of optical bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
■ First, follow the reaction tray dismantling procedure. See 1. Reaction tray dismantling, page 2.
■ Unscrew the 7 CHC screws, disconnect the flap door switch and unscrew the NTC to remove the
upper case. See 2.2. NTC replacement, page 5.
■ Follow the 2.4.3. Upper rollers replacement, page 10 procedure until you removed the holder disk.
■ Follow the 2.4.4. Down rollers replacement, page 13 procedure to remove the crown wheel.
■ Cut one ear of the new home sensor and twist the cables.
■ Install the new home sensor and center it in the notch.
■ Reassemble in reverse order.
When reinstalling the crown wheel, ensure that the home sensor does not touch the crown
wheel flag.
■ Check all the reaction tray position adjustments. See 4. Adjustments, page 19.
3. Impacted adjustments
4. Adjustments
The following table lists the functional positions to adjust. Those positions are reached by three different
types of adjustment:
- the combination of two movements to obtain a centering or
- performing an automatic "AUTO" adjustment or
- performing a manual "MAN" adjustment
The table also indicates the tool required to perform those adjustments.
Modules
Reaction Tray
Sector Position Target Type Tool
Optical Bench Light Beam
1 Offset AUTO
Mixer
Cuvette Position 1 2 Mixing Position
Reagent arm rotation
Cuvette Position 1 1 Reagent Arm Position
Sample arm rotation
+
Cuvette changer
Vertical: Motor Off;
Horizontal: Load in Reaction 1 1 Automatic Loading
Tray Position
Reaction tray
1 1 Handling Position MAN
Make sure that all the assemblies are at their home position before starting an adjustment.
Make sure that the arms are in the upper position before moving a tray.
■ Connect the power supply cable and switch the instrument on.
■ Go to Services > Diagnostics > Tray.
■ Beforestarting the position adjustments, select the position of the adjustment tool or cuvette segment
on the reaction tray:
This position adjustment is performed with an adjustment tool: OPTICAL, SEGMENT 1XXX TEST
9200787 (1229200787).
Make sure that the tool is loaded properly into the reaction tray. It is necessary to press the
tool completely down into the reaction tray.
A
B
The instrument evaluates the quality of the current ajdustment. If the current adjustment is not
satisfactory, a new offset is determined and the instrument carries out a second measure with this
new offset. If this new offset is not satisfactory, a new offset is again determined and the instrument
carries out a third measure.
D G
The calculated offset value is displayed in
the Calculated offset field (D):
- The value is displayed in green if it is within
range (optical density curve in green (G)).
- The value is displayed in red if it is out of
range (optical density curve in red (G)).
■ If
the adjustment is not correct, press E F
Cancel (F). The optical density curve and
the calculated offset are erased. Run
measure cycles until the adjustment is
correct.
■ If the adjustment is correct, press OK (E).
■ Leave the adjustment tool in the reaction tray to adjust the other positions.
■ If the home position is adjusted, the other positions have to be adjusted too.
This position adjustment is performed with an adjustment tool: OPTICAL, SEGMENT 1XXX TEST
9200787 (1229200787).
The position "2" of the adjustment tool will be used.
1 2
■ If the previous adjustment has been carried out, the adjustment tool is loaded in the reaction tray in
position "1". If not, manually load it. See 4.3.1. Adjustment tool installation, page 21.
Leave the adjustment tool in the reaction tray to adjust the other positions.
■ Replacethe reagent and sample needles respectively by the "Dummy reagent needle" (see RAS385:
Arms, 5.2. "Dummy reagent needle" installation, page 25) and the "Dummy sample needle" (see
RAS385: Arms, 6.2. "Dummy sample needle" installation, page 38).
Make sure that the sample arm is in its vertical home position before moving the reagent arm.
If the previous adjustment has been carried out, the adjustment tool is loaded in the reaction tray in
position "1". If not, manually load it. See 4.3.1. Adjustment tool installation, page 21.
The position "1" of the adjustment tool will be used.
1 2
The value of the rotation home offset (7) must not be modified.
Adjust the rotation home position with the reagent arm mechanical adjustment described
below.
This position corresponds to the home position. Therefore, the number of steps in the Target
scrolling list must be "0". This is fixed and must not be changed.
Follow this procedure to check the position only.
Make sure that the reagent arm is in its wash position (rotation and vertical) before moving
the sample arm.
If the previous adjustment has been carried out, the adjustment tool is loaded in the reaction tray in
position "1". If not, manually load it. See 4.3.1. Adjustment tool installation, page 21.
The position "2" of the adjustment tool will be used.
1 2
The value of the rotation home offset (6) must not be modified.
Adjust the rotation home position with the sample arm mechanical adjustment described
below.
■ First,
install the "Test segment Pentra 400". See RAS384: Cuvette changer, 4.2. "Test segment Pentra
400" installation, page 32.
■ Perform
the reaction tray adjustment. See RAS384: Cuvette changer, 4.4. Adjustment of reaction tray
"Automatic Loading" position, page 34.
■ Reinstall the reaction tray cover by slightly turning the 3 CHC screws and washers.
■ Reconnect the flap door switch.
Make sure that the sample arm is in its vertical home position before moving the reagent arm.
Make sure that the reagent arm is in its wash position (rotation and vertical) before moving
the sample arm.
■ Remove the "Dummy reagent needle" and the "Dummy sample needle" and put the reagent and
sample needles back.
This adjustment is described during the cuvette changer adjustment. See RAS384: Cuvette changer,
4.4. Adjustment of reaction tray "Automatic Loading" position, page 34.
Concerns
Reaction tray lower box dismantling
Fan replacement
Heater replacement
Impacted adjustments
Check up after intervention
Required tools
Hexagonal keys
Hexagonal screwdriver
Flat screwdriver
Phillips screwdriver
Pliers
Required products
None
Intervention time
N/A
Frequency
On request
In order not to damage the needles during dismantling, disable the arms (vertical and rotation
movements) and put them on a sample cup rack over the reagent tray as shown on the
following picture.
■ Switch the instrument off and disconnect the power supply cable.
■ Lift up the arms main cover and the mixer.
■ Remove the loader cover, the cuvettes hatch, the connection hatch, the cuvettes cover, the optic
hatch, the left arm cover, the cuvettes tray plate and the mixer plate. See RAS377: Covers
dismantling, page 1.
Collar
Collar
2. Fan replacement
■ First, perform the lower box dismantling. See 1. Reaction tray lower box dismantling, page 2.
Fan rotation
Air direction
(toward the heater) direction
Air direction
(toward the heater)
■ The thermic bulkhead notch must be placed in front of the spectrophotometer flat cable
notch (A).
■ When connecting the cooling unit tubings on the lower box, pay attention to connect the
Input and Output correctly (B).
Notch
Input Output
Before fastening the 4 CHC screws maintaining the lower box, ensure that the reaction tray
home sensor cable, the spectrophotometer flat cable, the fan cable and the heater cable are
well positioned in their respective notches.
Spectrophotometer
flat cable notch
Fan and heater notch
3. Heater replacement
■ First, perform the lower box dismantling procedure. See 1. Reaction tray lower box dismantling,
page 2.
Be careful when positioning the heater. The heater metallic flaps must be on top.
Fan rotation
Air direction
(toward the heater) direction
Air direction
(toward the heater)
■ The thermic bulkhead notch must be placed in front of the spectrophotometer flat cable
notch (A).
■ When connecting the cooling unit tubings on the lower box, pay attention to connect the
Input and Output correctly (B).
Notch
Input Output
Before fastening the 4 CHC screws maintaining the lower box, ensure that the reaction tray
home sensor cable, the spectrophotometer flat cable, the fan cable and the heater cable are
well positioned in their respective notches.
Spectrophotometer
flat cable notch
Fan and heater notch
4. Impacted adjustments
None.
■ Connect the power supply cable and switch the instrument on.
■ On the lower box, make sure that there is no leak at the level of Input and Output fittings.
Optical bench
Concerns
Optical bench dismantling
Optical bench mirror and lenses cleaning and replacement
Impacted adjustments
Optical bench check
Required tools
Hexagonal keys
Hexagonal screwdriver
Open-end wrench
Flat screwdriver
Phillips screwdriver
KIT, ANTISTATIC KIT MZZ015A (1207921015)
TOOL, OPT. BENCH CLEANING KIT XEA945BS (1209159945)
Required products
Dusting spray
Intervention time
N/A
Frequency
On request
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
1.1. Dismantling
In order not to damage the needles during dismantling, disable the arms (vertical and rotation
movements) and put them on a sample cup rack over the reagent tray as shown on the
following picture.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the loader cover, the cuvettes hatch, the connection hatch and the cuvettes cover.
- Lift the mixer assembly up by pressing the red button.
- Remove the optic hatch, the left arm cover, the cuvettes tray plate and the mixer plate.
- Remove the recuperation jar.
■ Follow the reaction tray dismantling procedure. See RAS382: Reaction tray, 1. Reaction tray
dismantling, page 2.
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 1.1.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 6.
At this stage of the procedure, you can dismantle the spectrophotometer as well as the
acquisition board although this is not necessary to finish the optical bench dismantling.
1.1.2. Specific procedure ABX Pentra 400 with an old model of optical
bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
The acquisition board dismantling procedure is described below but is not necessary to
dismantle the optical bench.
1.2. Reassembly
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 1.2.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 14.
■ Put the optical bench in place. Two dog points located under the optical bench ensure that you put it
in the correct position.
■ Reassemble the spectrophotometer as well as the acquisition board in reverse order. Do not forget to
put the ground wires back.
■ Put the spectrophotometer in place. The spectrophotometer gun must reach the end stop.
■ Reassemble the fan plate and the lamp supply cable support in reverse order.
■ Reassemble the lamp in reverse order.
Do not touch the glass part of the lamp with your fingers!
Make sure that the lamp is correctly positioned.
1.2.2. Specific procedure ABX Pentra 400 with an old model of optical
bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
■ Make sure that the spectrophotometer is correctly engaged in the optical bench.
Spectrophotometer NOT OK
Spectrophotometer OK
■ Reassemble the fan plate and the lamp supply cable support in reverse order.
■ Reassemble the lamp in reverse order.
Do not touch the glass part of the lamp with your fingers!
Make sure that the lamp is correctly positioned.
Take care not to touch the mirror or the lenses with your fingers. Wear gloves to handle the
mirror and the lenses.
2.1.1. Dismantling
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 2.1.1.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 18.
■ Follow the reaction tray dismantling procedure. See RAS382: Reaction tray, 1. Reaction tray
dismantling, page 2.
2.1.1.2. Specific procedure ABX Pentra 400 with an old model of optical bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
■ Follow the optical bench dismantling procedure. See 1.1. Dismantling, page 2.
Pushing the lens, take care not to touch the lens but the metallic part.
A B
Make sure that the pen with suction cup is clean before use.
If necessary, clean it with a cleaning towelette (provided in the optical bench cleaning kit).
■ Put the condensing lens back in its metallic support using the pen with suction cup and fasten the nut.
■ Remove any dust from the condensing lens using a dusting spray.
Make sure that there are no marks on the condensing lens.
2.1.3. Reassembly
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 2.1.3.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 22.
■ Put the lens holder back in its original position. Make sure that the convex side of the lens is facing
the right direction (opposite to the lamp side).
Make sure that the lens holder reaches the end stop so that it is properly placed.
CONDENSING LENS
focal length = 20 mm
2.1.3.2. Specific procedure ABX Pentra 400 with an old model of optical bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
■ Reassemble in reverse order the heat sink cover and the cap.
■ Clean the mirror with a cleaning towelette. Wipe the mirror with paper.
■ Remove any dust from the mirror using a dusting spray.
Make sure that there are no marks on the mirror.
■ Reassemble in reverse order the mirror.
■ Follow the optical bench reassembly procedure. See 1.2. Reassembly, page 12.
2.2.1. Dismantling
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 2.2.1.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 24.
■ Follow the reaction tray dismantling procedure. See RAS382: Reaction tray, 1. Reaction tray
dismantling, page 2.
2.2.1.2. Specific procedure ABX Pentra 400 with an old model of optical bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
■ Follow the optical bench dismantling procedure. See 1.1. Dismantling, page 2.
■ Remove any dust from the shaping lens using a dusting spray and make sure that there are no marks
on the shaping lens.
■ Put the shaping lens back in its metallic support using the pen with suction cup and tighten the screw.
SHAPING LENS
focal length = 25 mm
2.2.3. Reassembly
If your instrument is equipped with an old model of optical bench (before "XDA829C"), please
refer to the specific procedure: 2.2.3.2. Specific procedure ABX Pentra 400 with an old model
of optical bench (before "XDA829C"), page 26.
Make sure that the lens holder reaches the end stop so that it is properly placed.
2.2.3.2. Specific procedure ABX Pentra 400 with an old model of optical bench (before "XDA829C")
This procedure is designed for ABX Pentra 400 equipped with an old model of optical bench
(before "XDA829C") i.e. ABX Pentra 400 with an instrument serial number lower than 3195.
■ Follow the optical bench reassembly procedure. See 1.2. Reassembly, page 12.
■ Follow
the optical bench dismantling procedure until you dismantled the spectrophotometer. See 1.1.
Dismantling, page 2.
The coupling lens is located inside the reception barrel of the spectrophotometer.
To replace the coupling lens, you have to replace the reception barrel.
■ Put the coupling lens back in the reception barrel using the pen with suction cup and fasten the nut.
COUPLING LENS
focal length = 20 mm
■ Remove any dust from the coupling lens using a dusting spray and make sure that there are no marks
on the coupling lens.
■ Reassemble in reverse order.
■ Follow the optical bench reassembly procedure. See 1.2. Reassembly, page 12.
3. Impacted adjustments
These adjustments are necessary only if your instrument is equipped with an old model of
optical bench (before "XDA829C").
■ Run an initialization and once the instrument is Ready, go to Services > Diagnostics > Tray.
■ Select the Reaction radio button and press Motor Off.
■ Manually remove all the cuvette segments from the reaction tray.
■ Then, press Check Home.
1. Measure Gain
2. I Black
3. Lamp Stabilization
Then, the following message is displayed: "Verify absence of segment in sector 1."
■ Make sure that there is no cuvette segment in the sector 1 of the reaction tray and press OK.
During the lamp stabilization, the light intensity measured on air (without cuvette) and the deviation are
displayed for each wavelength every 12 s during 600 s maximum.
The light intensities (LI) are checked to ensure that they are included between 57200 and 65535.
The deviations (Dev) are checked to ensure that the difference between 2 consecutive absorbances
< 0.00022.
Once the step is performed, the following message is displayed: "Stability of lamp done."
4. I0 Air
5. I0 Water
■ Click the I0 Water tab (A).
C
■ Press Start (B).
Then, the following message is displayed:
"Put a new segment in sector 1 and
manually fill the first cuvette with 200 µL of
H2O in the handling position."
■ Manually load a cuvette segment into the
sector 1 of the reaction tray, manually fill the
first cuvette with 200 µL of H2O and press
OK. A
Once the step is performed, the light
intensity measured through a water-filled B
cuvette is displayed for each wavelength
(C).
Concerns
Preliminary operations
Optical bench lamp dismantling
Condensing lens cleaning (lamp side)
Checks after intervention
Required tools
Pair of scissors
TOOL, ALLEN SCREWDRIVER 2MM MAB086A (1207821086)
Required products
Alcohol
Intervention time
0 h 15
Frequency
On request
Follow this procedure to clean the lamp side of the condensing lens with the help of the
TOOL, LAMP LENS CLEANING KIT XEC011AS (1209179011) and without dismantling the
optical bench.
1. Preliminary operations
crystal tube
optic wipes
For a better handling of the tool, you can also put a crystal tube lenght at the other extremity
of the tool.
This crystal tube lenght is in the little bag, ref. EAE011A (1202241011), which contains about
10 cm of crystal tube.
■ Refer to your user manual to dismantle the lamp to access the condensing lens (lamp side).
Do not touch the glass part of the lamp with your fingers!
spectrophotometer
A B
■ Once the tool is correctly inserted, get in touch with the lens and clean it by making small rotational
movements and keeping the tool as vertical as possible.
As the lens surface is positioned further than the emission chamber walls, the lens contact is
perceptible.
■ Follow the optical bench check procedure (see RAS383: Optical bench, 4. Optical bench check,
page 31) to control the cleaning efficiency.
Mixer
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
RAS386: Mixer
Concerns
Mixer paddle replacement
Mixer assembly dismantling
Mixer assembly parts replacement
Impacted adjustments
Adjustments
Required tools
Hexagonal keys
Phillips screwdriver
OPTICAL, SEGMENT 1XXX TEST 9200787 (1229200787)
Required products
None
Intervention time
N/A
Frequency
On request
■ Connect the power supply cable and switch the instrument on.
When reassembling, make sure that the mixer paddle is pushed up to the maximum in its
support.
In order not to damage the needles during dismantling, disable the arms (vertical and rotation
movements) and put them on a sample cup rack over the reagent tray as shown on the
following picture.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the mixer cover.
■ Lift the mixer assembly up by pressing the red button.
■ Manually push down the cylinder to move the XY carriage up (A), then forward (B).
■ Cut the Ty-Rap™ maintaining the reagent arm vertical motor cable and gently remove the mixer
assembly.
■ When reassembling, turn the 6 CHC screws of the mixer assembly foot without tightening
them. Push the mixer assembly down and check if it is correctly engaged. Then, tighten the
6 CHC screws of the mixer assembly foot.
■ Be careful not to clamp the tubings and wires when you push the mixer assembly down.
■ After the mixer assembly replacement, it is necessary to readjust all the mixer positions.
See 5. Adjustments, page 17.
In case of mixer assembly replacement, dismantle the mixer paddle from the old mixer
assembly and reassemble it on the new mixer assembly. See 1. Mixer paddle replacement,
page 2.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the mixer cover.
■ Lift the mixer assembly up by pressing the red button.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the mixer cover.
■ Lift the mixer assembly up by pressing the red button.
When reassembling, make sure that you tighten the motor axis screw on the plane of the
motor axis.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the mixer cover.
■ Lift the mixer assembly up by pressing the red button.
B
■ Loosen the CHC screw (A) and remove the
mixer paddle by pulling it down.
■ Unscrew the 2 CHC screws to remove the
mixer paddle motor (B).
■ Replacethe mixer paddle motor and A
reassemble in reverse order.
70 mm +/- 3
105 mm +/- 3
When reassembling, make sure that the mixer paddle is pushed up to the maximum in its
support.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the mixer cover.
■ Lift the mixer assembly up by pressing the red button.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the mixer cover.
■ Lift the mixer assembly up by pressing the red button.
■ When reassembling, make sure that the CHC screw is right above the cylinder.
■ After
the cylinder spring replacement, make sure that the XY carriage moves down without
moving backward.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
Open the arms main cover.
■ Lift the mixer assembly up by pressing the red button.
After the "mixer present switch" replacement, it is necessary to make sure that it works
correctly. See RAS394: Sensors check and adjustment, 6. "Mixer present switch", page 7.
4. Impacted adjustments
5. Adjustments
Disable the arms (vertical and rotation movements) and put them on a sample cup rack over
the reagent tray as shown on the following figure.
■ Switch the instrument off and disconnect the power supply cable.
■ Open the arms main cover.
■ Remove the mixer cover, the loader cover, the cuvettes hatch, the connection hatch, the cuvettes
cover, the optic hatch, the left arm cover, the cuvettes tray plate and the mixer plate. See RAS377:
Covers dismantling, page 1.
■ Remove the unload rack, the load rack and the reaction tray cover. See RAS382: Reaction tray, 1.
Reaction tray dismantling, page 2.
■ Connect the power supply cable and switch the instrument on.
■ Lift the mixer assembly up by pressing the red button.
Before starting position adjustments, make sure that the CHC screw is right above the
cylinder.
A
■ Check the distance between the XY
carriage and the low carriage.
■ Adjustthis position to have 7 mm +/- 0.5
between the XY carriage and the low
carriage by moving the home flag (A).
- Move the home flag down to move the XY
carriage up. 7 mm +/- 0.5
- Move the home flag up to move the XY
carriage down.
■ Press Check Home (B), then check the
position again.
≈2 mm
■ Adjust the reaction tray Mixing Position position. See RAS382: Reaction tray, 4.4. Mixing Position,
page 23.
Follow this procedure to adjust the mixer paddle height in the cuvette.
The distance between the end of the mixer paddle and the bottom of the cuvette must be
3 mm.
3 mm
Follow this procedure to adjust the mixer paddle height above the reaction tray.
A
■ Go to Services > Diagnostics > Arms.
■ Select the
Mixer radio button (A) and press
Check Home (B). C
■ In
the Position scrolling list, select Above
Reaction Tray (C).
■ Press Check Position (D).
■ When the mixing paddle stops turning, B D E
press Motor Off (E).
Mixer hole
Arms
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
■ V2 corresponds to instruments with serial numbers between 2000 and 2999.
RAS385: Arms
Concerns
Needles replacement
Arms assembly dismantling
Arms assembly parts replacement
Impacted adjustments
Reagent arm adjustment
Sample arm adjustment
Level detection check
Shock detection check
Required tools
Hexagonal keys
Torx key
Flat screwdriver
Phillips screwdriver
TOOL, DYNAMO. SCREWDRIVER A302 MAG019A
(1207851019)
OPTICAL, SEGMENT 1XXX TEST 9200787 (1229200787)
TOOL, REAG TRAY ADJUSTING TOOL XDB097AS
(1209149097)
TOOL, DUMMY REAGENT NEEDLE GBM1124 (1203601124)
TOOL, DUMMY SAMPLE NEEDLE GBM1125 (1203601125)
Required products
Distilled water
TOOL, THREADLOCKING LAX003A (1207721003)
Intervention time
N/A
Frequency
On request
1. Needles replacement
■ Connect the power supply cable and switch the instrument on.
■ Go to Services > Customer Services > Cycles.
Be careful not to clamp the tubing and wires of the reagent arm when you fasten the reagent
arm bracket cover.
When reassembling, take care that the plastic collars are positioned in the correct way. See
the picture above.
■ Before the sample arm bracket cover reassembly: position, as much as possible, the
sample needle locking screw towards the sample arm inside.
■ Take care that the tubing is correctly positioned in the sample arm bracket cover and be
careful not to clamp the tubing nor the wires of the sample arm when you fasten the sample
arm bracket cover.
■ When the sample arm bracket cover is fastened, make sure that the shock detection runs
smoothly. See 8. Shock detection check, page 59.
■ Switch the instrument off and disconnect the power supply cable.
It is advisable to remove the needles before dismantling the arms assembly (in order not to
damage them).
■ Slightly lift the arms assembly up, then cut the Ty-Rap™ and disconnect the 2 home sensor
connectors (A) and the 2 rotation motors (B).
A
Specific ABX Pentra 400 V1
■ First,cut the Ty-Rap™ and disconnect the 2
home sensor connectors (A) and the 2
rotation motors (B).
Make sure that all the wiring is in the correct position before putting a new Ty-Rap™ and
make sure that the wires are not in the way of the home sensors.
This procedure describes how to replace the 2 vertical home sensors and the 2 rotation home
sensors:
- 3.1.1. Vertical home sensor, page 9
- 3.1.2. Rotation home sensor, page 11.
C
■ Cut the Ty-Rap™ (A) and disconnect the 2
vertical motor connectors (B).
■ Unscrew the CHC screw (C) to release the
vertical home sensor and its wires.
B
A
■ To ensure that the cable is correctly positioned, check the cable bend (refer to the following picture)
when the rack rail assembly is in low position.
Reagent arm Sample arm
■ Make sure that the home flag passes in the middle of the home sensor and does not touch the home
sensor. If necessary, manually adjust the home flag position.
This procedure describes how to replace the reagent and sample vertical motors and the
reagent and sample rotation motors:
- 3.2.1. Vertical motor, page 12
- 3.2.2. Rotation motor, page 14.
A
■ Remove the vertical home flag by
unscrewing the 2 CHC screws (A). B
A
■ Remove the end stop by unscrewing the 2
CHC screws (B).
■ Remove the wire guide support by B
unscrewing the 2 CHC screws (C).
C
On the reagent arm, before removing end stop screws, note the position of the screws on the
end stop to reassemble it in the same way.
When reassembling, put threadlocking LOCTITE 222 on the end of the 4 CHC screws. First
turn the 3 CHC screws and washers without tightening them. Then, turn the last CHC screw
with the spring and tighten the 4 CHC screws.
When reassembling, first turn the 4 CHC screws and washers without tightening them. Then,
fasten the belt tensioner screw at 90 mN.m with a dynamometric screwdriver and tighten the
4 CHC screws.
A
■ Remove the vertical home flag by
unscrewing the 2 CHC screws (A). B
A
■ Remove the end stop by unscrewing the 2
CHC screws (B).
■ Remove the wire guide support by B
unscrewing the 2 CHC screws (C).
C
belt
pulley
As the rack rail assembly is solidly built, you might have to pull it hard.
When reassembling the pulley, first fasten the pulley and put the belt back. Then, fasten the
belt tensioner screw at 90 mN.m with a dynamometric screwdriver and tighten the 4 CHC
screws and washers.
On the reagent arm, before removing the end stop screws, note the position of the screws on
the end stop to reassemble it in the same way.
belt
pulley
As the rack rail assembly is solidly built, you might have to pull it hard.
When reassembling the pulley, first fasten the pulley and put the belt back. Then, fasten the
belt tensioner screw at 90 mN.m with a dynamometric screwdriver and tighten the 4 CHC
screws and washers.
When reassembling the reagent arm, be careful to well position the CHC screws on the end
stop. Some end stops have 2 holes and others have 4 holes. Refer to the following picture to
know the correct positioning of the end stop screws.
■ Follow the arms assembly dismantling procedure. See 2. Arms assembly dismantling, page 7.
■ Disconnect the 2 connectors from the reagent level detection board (J2 and J4) or the connector from
the sample level detection board (J2).
■ Remove the reagent or sample rack rail assembly carefully in order not to clamp and not to damage
the cables. See 3.3. Reagent or sample rack rail assembly replacement, page 14.
Arm notch
Ty-Rap™
4. Impacted adjustments
The indications in the following table have to be taken into account only if a preliminary
adjustment with the TOOL, REAG TRAY ADJUSTING TOOL XDB097AS (1209149097) has
been performed by the factory or during a previous intervention.
If it is not the case, it is imperative to perform all the adjustments of the functional positions
mentioned.
Sample arm
Reagent arm
The following table lists the functional positions to be adjusted. Those positions are reached by three
different types of adjustments:
- the combination of two movements to obtain a centering or
- performing an automatic "AUTO" adjustment or
- performing a manual "MAN" adjustment
The table also indicates the tool required to perform those adjustments.
Modules
Reagent Arm Rotation
Sector Position Position Type Tool
Reaction tray
Reagent tray
R1 Pos.-Reagent Rack for Reagent arm 1-A R1 Pos.-Reagent Rack
2
R2 Pos.-Reagent Rack for Reagent arm 2-A R2 Pos.-Reagent Rack
Reagent Rack
R3 Pos.-Reagent Rack for Reagent arm 3-A R3 Pos.-Reagent Rack
R1 Pos.-Cassette for Reagent arm 1 1 R1 on Cassette
R2 Pos.-Cassette for Reagent arm Cassette 2 R2 on Cassette
Modules
Reagent Arm Vertical
Sector Position Position Type Tool
Reaction tray
Reagent tray
■ Before starting the position adjustments, remove the covers (see RAS377: Covers dismantling,
page 1):
- Open the arms main cover.
- Remove the external and internal sample covers, then remove the optic hatch.
- Lift the mixer up, then unscrew the 2 CHC screws of the left arm cover.
- Remove the cuvettes tray plate, the cuvettes hatch and the arm bracket covers.
■ Connect the power supply cable and switch the instrument on.
■ Press Stop to stop the initialization.
Always move the sample arm to its upper position (vertical home position) before moving the
reagent arm.
Always move the sample and reagent arms to their upper positions (vertical home position)
before moving any tray.
■ Perform the reagent needle dismantling. See 1.1. Reagent needle replacement, page 2.
■ Install
the "Dummy reagent needle" on the
reagent arm.
2 10
1
A
■ Go to Services > Diagnostics > Tray.
■ Select the Reaction radio button (A).
C
■ Press Check Home (B).
■ Inthe Sector and Position scrolling lists,
select "1" and "1" (C). D
■ In
the Target scrolling list, select Handling
Position (D).
B E
■ Press Check Position (E).
■ Load the tool into the reaction tray.
Make sure that the tool is loaded properly in the reaction tray. It is necessary to press the tool
completely down in the reaction tray.
"Cuvette Position"
■ The rotation adjustment value for the Cuvette Position position is factory adjusted on the
rotation home position, therefore, the number of steps for the Cuvette Position position is
0. This is fixed and must not be changed.
■ If the rotation home position is adjusted, the other positions have to be adjusted too.
Follow this procedure to have the reagent needle centered in the cuvette.
The value of the rotation home offset (5) must not be modified.
Adjust the rotation home position with the mechanical adjustment described below.
Follow this procedure to have the reagent needle centered in its wash tower.
Follow this procedure to adjust the reagent needle height in the cuvette.
The point of the needle must be 2 mm above the bottom of the cuvette.
2 mm
Follow this procedure to adjust the reagent needle height in its wash tower.
The distance between the underside of the reagent arm and the top of the wash tower must
be 91 mm +/- 0.5.
91 mm +/- 0.5
Follow this procedure to adjust the reagent needle height in the vial ("Low Position in
Reagent/Cal/Ctrl Rack") and in the cassette ("Low Position in Cassette").
The point of the needle must be 1 mm above the bottom of the vial and 1 mm above the
bottom of the cassette.
Vial Cassette
1 mm 1 mm
These two adjustments are made automatically, in only one go. See "ABX Cassette" (without level
detection), page 33.
The vertical position adjustment in a cassette is the same for both R1 and R2.
We will do the position adjustment for R1.
■ Move the "Reag tray adjusting tool" to the R1 Pos.- Cassette for Reagent Arm position.
To load the "Reag tray adjusting tool" on the reagent tray and to move it to the R1 Pos.-
Cassette for Reagent Arm position, see RAS380: Reagent tray, 4.3. Preliminary procedure,
page 23.
■ In
the Reference point scrolling list, select 6
ABX Cassette (6).
■ Press Check Position (3).
■ Then, use the + and/or - buttons to adjust
the position of the "Dummy reagent
needle".
- + = Increase the number of steps to move
the reagent arm down. 3
- - = Decrease the number of steps to move
the reagent arm up.
Place the reagent arm in low position in the wash tower before moving the sample arm.
See 5.4.2. "Low Position in Wash Tower", page 32.
The following table lists the functional positions to be adjusted. Those positions are reached by three
different types of adjustments:
- the combination of two movements to obtain a centering or
- performing an automatic "AUTO" adjustment or
- performing a manual "MAN" adjustment
The table also indicates the tool required to perform those adjustments.
Modules
Sample Arm Rotation
Sector Position Position Type Tool
Reaction tray
Reagent tray
R1 Pos.-Reagent Rack for Sample arm 1-A R1 Pos.-Reagent Rack
2
R2 Pos.-Reagent Rack for Sample arm 2-A R2 Pos.-Reagent Rack
Reagent Rack
R3 Pos.-Reagent Rack for Sample arm 3-A R3 Pos.-Reagent Rack
R1 Pos.-Cal/Ctrl Rack for Sample arm 1 R1 Pos.-Cal/Ctrl Rack
3
R2 Pos.-Cal/Ctrl Rack for Sample arm 2 R2 Pos.-Cal/Ctrl Rack
Cal/Ctrl Rack
R3 Pos.-Cal/Ctrl Rack for Sample arm 3 R3 Pos.-Cal/Ctrl Rack
R1 Pos.-Cassette for Sample arm 1 1 R1 on Cassette
R2 Pos.-Cassette for Sample arm Cassette 2 R2 on Cassette
Sample tray
External Sampling Pos. 1 2 External Sample
Internal Sampling Pos. 1 1 Internal Sample
ISE Tower ISE Sample
Modules
Sample Arm Vertical
Sector Position Position Type Tool
Reaction tray
Reagent tray
■ Perform the sample needle dismantling procedure. See 1.2. Sample needle replacement, page 4.
■ Install
the "Dummy sample needle" on the
sample arm.
2 10
1
It is necessary to load this adjustment tool in the reaction tray. Follow the procedure described in
Adjustment tool installation, page 26.
"Cuvette Position"
■ The rotation adjustment value for the Cuvette Position position is factory adjusted on the
rotation home position, therefore, the number of steps for the Cuvette Position position is
0. This is fixed and must not be changed.
■ If the rotation home position is adjusted, the other positions have to be adjusted too.
Follow this procedure to have the sample needle centered in the cuvette.
A
■ Go to Services > Diagnostics > Tray.
■ Select the Reaction radio button (A).
C
■ Press Check Home (B).
■ Inthe Sector and Position scrolling lists,
select "1" and "2" (C). D
■ In
the Target scrolling list, select Sample
Arm Position (D). E
B
■ PressCheck Position to move the tool to
the Sample Arm Position position (E).
The value of the rotation home offset (4) must not be modified.
Adjust the rotation home position with the mechanical adjustment described below.
arm adjustment
Follow this procedure to have the sample needle centered in its wash tower.
Ensure that the sample arm is at its vertical and rotation home position.
Follow this procedure to center the sample needle in the ISE mix cup.
Ensure that the sample arm is at its vertical and rotation home position.
2 mm
Ensure that the sample arm is at its vertical and rotation home position.
Take care of the shock detection. It should not be activated otherwise the adjustment won’t
be correct.
Follow this procedure to adjust the sample needle height in its wash tower.
The distance between the underside of the sample arm and the top of the wash tower must
be 111 mm +/- 0.5.
Ensure that the sample arm is at its vertical and rotation home position.
Follow this procedure to adjust the sample needle height in the vial ("Low Position in Reagent
rack"), in the sample cup ("Low position CalCs on reagent tray") and in the cassette ("Low
Position in Cassette").
The point of the needle must 1 mm above the bottom of the vial, 1 mm above the bottom of
the sample cup and 1 mm above the bottom of the cassette.
1 mm 1 mm 1 mm
These three adjustments are made automatically, in only one go. See "ABX Cassette" (without level
detection), page 47.
Ensure that the sample arm is at its vertical and rotation home position.
The vertical position adjustment in a cassette is the same for both R1 and R2.
We will do the position adjustment for R1.
■ Move the "Reag tray adjusting tool" to the R1 Pos.- Cassette for Sample Arm position.
To load the "Reag tray adjusting tool" on the reagent tray and to move it to the R1 Pos.-
Cassette for Sample Arm position, see RAS380: Reagent tray, 4.3. Preliminary procedure,
page 23.
■ In
the Reference point scrolling list, select
ABX Cassette (6).
■ Press Check Position (3).
6
■ Then, use the + and/or - buttons to adjust
the position of the "Dummy sample needle".
- + = Increase the number of steps to move
the sample arm down.
3
- - = Decrease the number of steps to move
the sample arm up.
Take care of the shock detection. It should not be activated otherwise the adjustment won’t
be correct.
Follow this procedure to adjust the sample needle height in the sample cup ("Low Position in
Sample Cup") and in the sample tube ("Low Position in Sample Tube").
The point of the needle must be 1 mm above the bottom of the sample cup and 1 mm above
the bottom of the sample tube.
1 mm 1 mm
These two adjustments are made automatically, in only one go. See "Sample tube rack" (without level
detection), page 50.
Ensure that the sample arm is at its vertical and rotation home position.
The vertical position adjustment in a sample tube is valid and is the same for both the
External Sample and Internal Sample positions.
We will do the position adjustment for the Internal Sample position.
To load a sample rack on the sample tray in position "1" and to move the position "1" of this
sample rack to the Internal Sampling Pos. position, see RAS381: Sample tray, 4.2.
Preliminary procedure, page 17.
■ In
the Reference point scrolling list, select
Sample tube rack (6).
■ Press Check Position (3).
6
■ Then, use the + and/or - buttons to adjust
the position of the "Dummy sample needle".
- + = Increase the number of steps to move
the sample arm down.
3
- - = Decrease the number of steps to move
the sample arm up.
Take care of the shock detection. It should not be activated otherwise the adjustment won’t
be correct.
Follow this procedure to adjust the sample needle height in the ISE mix cup.
The distance between the underside of the sample arm and the top of the ISE mix cup must
be 121 mm +/- 0.5.
Ensure that the sample arm is at its vertical and rotation home position.
■ In
the Reference point scrolling list, select
ISE (7).
■ Press Check Position (3).
■ Then, use the + and/or - buttons to adjust
the position of the "Dummy sample needle". 7
The end of the "Dummy sample needle"
must be positioned right above the upper
part of the ISE mix cup, this position is used
as vertical reference position.
3
- + = Increase the number of steps to move
the sample arm down.
- - = Decrease the number of steps to move
the sample arm up.
Take care of the shock detection. It should not be activated otherwise the adjustment won’t
be correct.
■ Remove the "Dummy sample needle" and the "Dummy reagent needle" and put the sample and
reagent needles back.
The principle of this procedure is to move the reagent arm down until it detects the liquid in
the vial.
To load a reagent rack on the reagent tray and to move the position R1 / A of this reagent rack
to the R1 Pos.- Reagent Rack for Reagent Arm position, see RAS380: Reagent tray,
page 1.
■ Ensure that the sample arm is at its vertical and rotation home position.
■ Ensure that the reagent arm is at its vertical and rotation home position.
In case of a problem, see Section 4: Electric and electronic principles, 3.3. Reagent level
detection board, page 4-20 to check the reagent level detection board (LEDs state).
The principle of this procedure is to move the sample arm down until it detects the liquid in
the vial.
To load a reagent rack on the reagent tray and to move the position R1 / A of this reagent rack
to the R1 Pos.- Reagent Rack for Sample Arm position, see RAS380: Reagent tray, page 1.
■ Ensure that the sample arm is at its vertical and rotation home position.
■ Ensurethat the reagent arm is in its wash tower. See 5.4.2. "Low Position in Wash Tower",
page 32.
In case of a problem, see Section 4: Electric and electronic principles, 3.2. Sample level
detection board XAA486AS (1209108486), page 4-18 to check the sample level detection
board.
The principle of this procedure is to move the sample arm down until it detects the bottom of
the vial.
■ Replace the hall-filled vial on the reagent rack with an empty one.
Cuvette changer
In this procedure, specific instructions are given for previous ABX Pentra 400 hardware
versions:
■ V1 corresponds to instruments with serial numbers below 2000.
Concerns
Cuvette changer racks dismantling
Cuvette changer parts replacement
Impacted adjustments
Adjustments
Required tools
Hexagonal keys
Torx key
Phillips screwdriver
TOOL, DYNAMO. SCREWDRIVER A302 MAG019A
(1207851019)
TOOL, TEST SEGMENT XDA893A (1209131893)
Required products
None
Intervention time
N/A
Frequency
On request
In order not to damage the needles during dismantling, disable the arms (vertical and rotation
movements) and put them on a sample cup rack over the reagent tray as shown on the
following picture.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the loader cover, the cuvettes hatch, the connection hatch and the cuvettes cover.
- Lift the mixer assembly up by pressing the red button.
- Remove the optic hatch, the left arm cover, the cuvettes tray plate and the mixer plate.
■ Remove the unload rack.
■ Remove the load rack as follows:
- Open the 2 adhesive collars and release the wires of the "rack used segment full" sensor.
- Disconnect the "rack used segment full" sensor (C19) and unscrew the 6 CHC screws.
On the instruments equipped with centering pins on the load rack support, the readjusting is
not mandatory. For the other instruments: see 3. Impacted adjustments, page 30.
■ Switch the instrument off and disconnect the power supply cable.
Vertical sensors
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the loader cover, the cuvettes hatch, the connection hatch and the cuvettes cover.
■ Replace the cuvette changer vertical sensor (home and/or low position) by following the corresponding
procedure.
C17
When reassembling, fasten the low position sensor in its lowest position.
■ Switch the instrument off and disconnect the power supply cable.
motor connector
■ Disconnect the motor connector.
■ Unscrew the 2 CHC screws to remove the
motor.
■ Replace the motor and reassemble in
reverse order.
motor screws
When reassembling, take care that the motor connector is correctly positioned.
General procedure
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
Remove the loader cover, the cuvettes hatch, the connection hatch and the cuvettes cover.
■ Remove the unload rack.
■ Remove the rear plates by unscrewing the 14 CHC screws to access the cuvette changer vertical
motor.
V5
V4
V3
2
- Remove the motor and the endless screw.
■ Replace the motor and the endless screw and reassemble in reverse order.
V5
V4
V3
■ Remove the motor assembly taking care not to drop the endless screw down.
■ Replace the motor assembly and reassemble in reverse order.
■ Ensure that you tighten the upper screw of the motor/endless screw coupling in the endless
screw notch.
■ Take care that the motor connector is correctly positioned.
■ Take care not to clamp the tubings when reassembling the manifold.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the loader cover.
■ Remove the unload rack.
■ Check if the cuvette changer carriage assembly has two or four silent blocks.
■ If the cuvette changer carriage assembly already has four silent blocks, replace them by
referring to the General procedure: four silent blocks, page 12.
■ If the cuvette changer carriage assembly has only two silent blocks, you must install the
whole KIT, SILENT BLOCK CARRIAGE ASSY XEC205AS (1209179205) by referring to the
Specific procedure: two silent blocks, page 13.
J20
free connector
A
When reassembling, take care to the position of the 2 connectors of the "rack used segment
in position" sensor.
A B
■ Take the new carriage assembly block (provided in the KIT, SILENT BLOCK CARRIAGE ASSY
XEC205AS (1209179205)).
- Fasten the 4 new silent blocks.
- Take the new nut support and install the nut in its support.
- Reassemble the nut and its support without tightening the support on the new carriage assembly
block.
- Reassemble the anti-twist bearing without tightening it.
- Reassemble in reverse order the two angle brackets and the carriage assembly plate.
■ Reassemble in reverse order the cuvette changer carriage assembly.
General procedure
■ Follow the cuvette changer racks dismantling procedure. See 1. Cuvette changer racks dismantling,
page 2.
In order not to lose the balls, never remove the carriage from the rail.
■ Dismantle the horizontal home flag from the new grabber assembly.
■ Replace the grabber assembly and reassemble in reverse order.
When reassembling, take care to the position of the rail: the end of the rail must be at the level
of the plate.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover.
- Remove the loader cover.
■ Remove the unload rack.
■ Follow the cuvette changer racks dismantling procedure. See 1. Cuvette changer racks dismantling,
page 2.
■ Remove the mother board cover (see RAS377: Covers dismantling, page 1) to access the "main cover
closed" sensor.
free connector
When reassembling, take care to the position of the 2 connectors of the "rack used segment
in position" sensor.
A A A
General procedure
■ Follow the cuvette changer racks dismantling procedure. See 1. Cuvette changer racks dismantling,
page 2.
■ Turn the load rack over to access the cuvette motion motor.
■ Replace the cuvette motion motor assembly and reassemble in reverse order.
When reassembling, first turn the 8 screws without tightening them. Then, tighten the 8
screws.
■ Assemble the two new iron corners. Do not tighten the screws.
■ Putthe new load rack assembly in place using the centering pins and reconnect the connectors in
reverse order.
■ Screw the load rack assembly on the computer. Do not tighten the screws.
■ Then, screw the load rack assembly on the iron corners. Do not tighten the screws.
B
B
C38 A
B
B
The connectors of the "rack used segment full" sensor (C19) and the "new segment
available" sensor (C38) have been modified.
■ In ABX Pentra 400 V1: it is necessary to use the "Cable, adaptor sensor rack" (provided in
the sensor kit) to connect the sensor to the right cable (linked to the mother board).
■ Ifthe instrument has a serial number anterior to #133: before installing the adaptor, it is
mandatory to replace the 4 points connectors C19 (for the unload rack) and C38 (for the
load rack) by new ones with 3 points. Proceed as follows:
- Disconnect the male and female parts of the connector.
- Replace the 4 points female connector by the new 3 points connector (provided in the
sensor kit):
Connect the first pin (which was in position 1 on the 4 points connector) in position 1 on the
new connector. Connect the second pin in position 2. Do not disconnect the third pin.
Connect the fourth pin in position 3. Cut the third wire end: cut the 4 points female
connector.
See picture on next page.
- Reconnect the male and female parts of the connector.
3 points connector
pos.3
pos.2
pos.1
3rd pin
pos.4
pos.3
pos.2
pos.1
4 points connector
3. Impacted adjustments
4. Adjustments
Follow the procedures 4.2. "Test segment Pentra 400" installation, page 32 and 4.3. Grabber
mechanical adjustment, page 33 before proceeding to the adjustments.
When you adjust a position by changing the number of steps for this position, press Check
Home, then check the position again (press Check Position) to validate and save the new
adjustment.
4.1. Introduction
The following procedure is used to adjust the cuvette segment loading/unloading mechanism and the
different grabber positions:
The adjustments of the reaction tray, the grabber horizontal and vertical positions, and the rack rails
positions are performed with an adjustment tool: TOOL, TEST SEGMENT XDA893A (1209131893).
■ Connect the power supply cable and switch the instrument on.
The purpose of this mechanical adjustment is to adjust the grabber orientation in the reaction
tray.
Each time you have to manually move the grabber, you must use the endless screw (vertical
movement) and the grabber gear wheel (horizontal movement).
The purpose of this adjustment is to obtain a correct cuvette segment loading in the reaction
tray. The adjustment is done by changing the number of steps for the reaction tray Automatic
Loading position.
■ Manually move the grabber to remove the "Test segment Pentra 400" from the reaction tray.
Before changing the number of steps for the reaction tray Automatic Loading position,
manually move the grabber to remove the "Test segment Pentra 400" from the reaction tray.
C
■ Selectthe Horizontal Motions > Load in
Reaction Tray Position position (A) and
press Check Position (B). A
■ Selectthe Vertical Motions radio button
(C) and press Check Home (D).
■ Put the reaction tray cover back.
D B
Make sure that the reagent and sample needles as well as the mixer paddle do not touch the
reaction tray cover.
E A
■ Select the Horizontal Motions radio button
(A) and press Check Home (B).
C locating pin
■ Select the Vertical Motions > Pause
Position Above Reaction Tray position (C)
and press Check Position (D).
B D
Make sure that the cuvette segment does not touch the reaction tray cover when you press
the cuvette segment down.
■ When the grabber is in this position, the vertical home flag should not cut the beam of the vertical low
position sensor. For this, make sure that the voltage on the connector C61 Pin 1-3 is < 1 V. If not,
readjust the position by lightly moving the grabber upwards.
■ Select the Vertical Motions radio button (E) and press Check Home (B).
■ Remove the cuvette segment from the grabber.
C E
■ Disable the cuvette changer vertical and
horizontal motors as follows:
- Select the Vertical Motions radio button
(C) and press Motor Off (D).
- Select the Horizontal Motions radio
button (E) and press Motor Off (D).
D
3 1 5
6 4 2
After a Vertical Motions > Check Home, the grabber moves to the Vertical Motions > New
Cuvette Holder Position position, then the grabber does not move when you select the
Vertical Motions > New Cuvette Holder Position position and press Check Position.
C A
C A
■ Select the Horizontal Motions radio button
(A) and press Check Home (B).
■ Select the Vertical Motions radio button
(C) and press Check Home (B).
■ Remove the cuvette segment from the load
rack.
B
A C
■ Disable the cuvette changer vertical and
horizontal motors as follows:
- Select the Vertical Motions radio button
(A) and press Motor Off (B).
- Select the Horizontal Motions radio
button (C) and press Motor Off (B).
B
C A
A C
■ Disable the cuvette changer vertical and
horizontal motors as follows:
- Select the Vertical Motions radio button
(A) and press Motor Off (B).
- Select the Horizontal Motions radio
button (C) and press Motor Off (B).
B
If you cannot do this preliminary adjustment correctly, readjust the unload rack rail.
See Unload rack rail adjustment, page 43.
If the gap between the end of the unload rack rail and the cuvette segment is higher than
2.5 mm, the unload rack will not be able to store 30 cuvette segments.
C A D
■ Selectthe Horizontal Motions radio button
(A) and press Check Home (B).
■ Selectthe Vertical Motions radio button
(C) and press Check Home (B).
■ Select the
Cuvette Motion radio button (D)
and press Check Home (B).
B
A
■ Go to Services > Diagnostics > Tray.
■ Disable the reaction tray as follows:
Select the Reaction radio button (A) and
press Motor Off (B).
■ Make sure that there is no cuvette segment
in the reaction tray. If necessary, manually
remove the cuvette segments.
■ Selectthe Reaction radio button (A) and C B
press Check Home (C).
Internal computer
Concerns
Computer dismantling
Ferrites installation (for computer models from "CCC014H")
Computer parts replacement
Required tools
Hexagonal keys
Open-end wrench
Flat screwdriver
Phillips screwdriver
KIT, ANTISTATIC KIT MZZ015A (1207921015)
Required products
None
Intervention time
1 h 00
Frequency
On request
1. Computer dismantling
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover and the ISE cover.
- Remove the external and internal sample covers, the power supply cover and the optic hatch.
■ Disconnect the mouse and the keyboard as well as the other computer connections.
■ Carefully
pull, then lift the computer
assembly.
■ Unscrew the CHC screw and washer
maintaining the power supply cable.
1 2 3
■ Disconnect the power supply cable (1), the
mother board cable (2), the RS232 cable (3)
and, if necessary, the printer cable (4).
■ Then, remove the computer assembly. Computer models < 1300013734
1 2 3
For computer models from "CCC014H", please ensure that the power supply cable is
equipped with two ferrites (one close to the computer assembly and another close to the
power supply).
See 2. Ferrites installation (for computer models from "CCC014H"), page 5.
Be very careful when you put back the cover of the computer fan box because you can touch/
disconnect the little board, shown on the following picture, with the cover (depending on the
computer model).
Please note that computer models from 1300013734 are no longer equipped with PS/2 ports
(mouse, keyboard) or parallel port (printer).
All the peripherals (mouse, keyboard, printer) should be connected into the USB ports.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
- Open the arms main cover and the ISE cover.
- Remove the external and internal sample covers, the power supply cover and the optic hatch.
ferrite
■ New shielded power supply cable
- Open the ferrite.
- Place the power supply cable in the ferrite.
- Make a loop with the power supply cable,
then close the ferrite.
If needed, to access the power supply cable, dismantle the power supply by referring to the
procedure RAS390: Power supply replacement, page 1.
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
As several computer models are available, a label, stuck on the rear plate, allows you to identify the
computer model.
This label can be read from the optic hatch opening with the help of a flashlight, without
dismantling the computer assembly first.
The table below lists the computer assembly spare parts and indicates their compatibility with the
different computer models in the field.
XAA511BS XEC074AS
CCC014A->F N/A N/A CBT018A N/A N/A N/A
(1209109511) (1209179074)2
XAA511BS XEC074AS
CCC014G->H P4-0853 N/A CBT018A N/A N/A N/A
(1209109511) (1209179074)2
XAA511BS
CCC014J P4-2166 N/A CBT018A 1201772017 N/A N/A N/A
(1209109511)
XAA511BS
CCC014K P4-2349 N/A CBT018A 1201772017 N/A N/A N/A
(1209109511)
XAA511BS CBT021A
CCC014L P4-3214 N/A 1201772017 N/A N/A N/A
(1209109511) (1201771021)
XAA511BS CBT021A
CCC014M P4-3391 N/A 1201772017 N/A N/A N/A
(1209109511) (1201771021)
P4-4000 / XAA511BS CBT021A
CCC014N N/A 1201772017 N/A N/A N/A
C4-0110 (1209109511) (1201771021)
1Please note that the computer assembly may have been changed on the instrument. In this case, do
not take into account the instrument serial # mentioned above.
2
Obsolete when sold out.
■ The hard drive is not loaded with the Windows master P400/C400.
Therefore, you have to install the Windows master P400/C400 by referring to the procedure
RAS533: Windows master installation, page 1.
■ Then, you have to install the software version and the reagent applications by referring
respectively to the procedures RAS517: Software version installation, page 1 and RAS518:
Reagent applications installation, page 1.
■ Press OK.
■ Touch each of the four corners of the screen to calibrate the touchscreen.
■ Press Apply, then OK.
A B
A B
When you disconnect (or reconnect) the flat cable (B) from the bottom angle plate, take care
not to disconnect this flat cable from the daughter board or the daughter board from the
mother board.
■ Unscrew the 4 CHC screws and washers maintaining the "hard drive + CD-ROM drive" assembly.
When reassembling, do not tighten the different screws too much in order not to damage the
hard drive or the CD-ROM drive.
For the IDE hard drive, ensure that the flat cable is correctly plugged into the hard drive
because 4 pins must be free.
■ The hard drive is not loaded with the Windows master P400/C400.
Therefore, you have to install the Windows master P400/C400 by referring to the procedure
RAS533: Windows master installation, page 1.
■ Then, you have to install the software version and the reagent applications by referring
respectively to the procedures RAS517: Software version installation, page 1 and RAS518:
Reagent applications installation, page 1.
WARNING! Take care to clear the way of the 2 fans: no flat cables in front of the fans
(overheating risk).
■ Unscrew
the 2 CHC screws to release the
CD-ROM drive.
■ Ensure that the flat cable is correctly plugged into the hard drive because 4 pins must be
free.
■ Do not tighten the different screws too much in order not to damage the hard drive or the
CD-ROM drive.
blank supports
■ Ensure that the brown band on the flat cable is in the correct position.
■ Do not forget to block the connector.
A white windows appears, with a red cross in the left upper corner.
■ Press this cross, it will move to the next position.
■ Pressthe red cross for the 9 positions, then press Enter twice.
The touch screen is calibrated.
Concerns
Power supply replacement
Power supply LEDs check
Required tools
Hexagonal keys
Phillips screwdriver
Voltmeter
KIT, ANTISTATIC KIT MZZ015A (1207921015)
Required products
None
Intervention time
0 h 30
Frequency
On request
■ Switch the instrument off and disconnect the power supply cable.
■ Open the arms main cover.
■ Remove the sample covers, the power supply cover, the optic hatch and the reagent cover. See
RAS377: Covers dismantling, page 1.
If the ABX Pentra 400 is not equipped with reinforced power supply cable:
If the ABX Pentra 400 is not equipped with reinforced power supply cable, connect the three
supply connectors after power supply installation.
■ Install
the new power supply with the
recuperation jar. The larger part of the
recuperation jar is positioned under the
reagent tray motor.
■ Reassemble in reverse order.
Recuperation jar
If the reagent tray has been lifted up, check all the centering positions of the reagent and
sample arms using the "Reag tray adjusting tool", the "Dummy reagent needle" and the
"Dummy sample needle". See RAS385: Arms, page 1.
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
■ Connect the power supply cable and switch the instrument on.
■ Remove the mother board cover. See RAS377: Covers dismantling, page 1.
Checking LEDs is enough. It is recommended not to check voltages with a voltmeter in order
not to damage the board (in fact, the test points are really small and the risk of a shortcut is
high).
Ground
■ If
one of the LEDs is not lit, use a voltmeter
point to check the corresponding voltage on
the connector.
■ Put the covers back.
-5V
+ 24 V
+5V +5V
Concerns
Parameters backup and software version check
Mother board replacement
Embedded software version installation
Restore parameters
Check up
Required tools
Hexagonal keys
KIT, ANTISTATIC KIT MZZ015A (1207921015)
Required products
None
Intervention time
1 h 00
Frequency
On request
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
Before changing the board, to save all mechanical parameters (offset values, stepper motor values, etc.),
proceed as follows:
Check the software version currently installed on the instrument. At the end of the procedure, you will
need to install the same software version.
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the mother board cover. See RAS377: Covers dismantling, page 1.
■ Carefully disconnect all the connectors from the mother board.
■ Unscrew the 9 CHC M4 screws to remove the board from its plate.
■ Install the new mother board on the plate and fasten the 9 CHC M4 screws.
■ Connect all the connectors on the board (see Section 4: Electric and electronic principles, 1.4. Mother
board connections, page 4-9).
It is necessary to reinstall the software version embedded on the mother board (flash memory
Eprom) because the latest software version has not been loaded on the new mother board.
■ Connect the power supply cable and switch the instrument on.
■ Afterthe boot of the operating system (Windows progress bar), the screen becomes black, then blue.
When the screen is blue, press Shift until the Windows login screen appears.
The left Shift key used to skip the automatic logon is no more functional under Windows 7.
Press CTRL+ALT+DEL keys to logoff and change current user.
■ Makesure that the following options are selected, if not select them:
Download P400 Eprom
Create a desktop icon.
■ When choosing the type of installation, select Update in order not to lose the configuration
(applications, calibrators, controls, settings, etc.) neither the patient results.
4. Restore parameters
To restore all mechanical parameters on the new board, please proceed as follows:
■ At the end of the instrument start, an error message appears which demands to restore the
parameters.
The following screen appears:
■ Click
OK on the following screen.
The parameters are restored.
5. Check up
■ Afterhaving restored parameters, it is advisable to check the mechanical adjustments. See RAS378:
6 month maintenance, 6. To check the mechanical adjustments, page 5.
■ Follow the "Check up after intervention" procedure. See RAS393: Check up after intervention, page 1.
Concerns
Reagent and sample syringes home sensors
Reagent tray home sensor
Sample tray home sensor
Reaction tray home sensor
Mixer assembly motor home sensor
"Mixer present switch"
Reagent and sample arms home sensors
Rack used segment (in position/full) sensors
"New segment available" sensor
Cuvette motion home sensor
Cuvette changer horizontal motions home sensor
Cuvette changer vertical motions home sensor
"Handling cover cuvette segment closed" sensor
"Main cover closed" sensor
Needle heating sensor
Reaction heating sensor
Refrigerated area sensor
Inner temperature sensor
"Handling cover reagent closed" sensor
Water tank empty sensor
Waste tank full sensor
Sample arm shock detection switch
Computer wake up sensor
Lamp power standby
Lamp power full
Low liquid level (cooling unit)
Power correct
Required tools
Hexagonal keys
Flat screwdriver
Phillips screwdriver
■ Remove the rear plate by unscrewing the 4 sample syringe reagent syringe
CHC screws to access the syringes home home sensor home sensor
sensors.
No adjustment available.
C
■ Select the Sample radio button (C), then
press Check Home to move the sample
syringe to its home position.
■ Make sure that the Home light (D) becomes D
green.
B
■ Go to Services > Diagnostics > Tray.
■ Select the Reaction radio button (A), then
press Check Home to move the reaction
tray to its home position.
■ Make sure that the Home light (B) becomes
green.
If one of the positions is not correct, adjust the "mixer present switch" as follows:
Unscrew the 2 CHC screws maintaining the switch, then move it up if the mixer assembly is
not detected in low position (red light) or move it down if the mixer assembly is detected in
high position (green light).
rotation home
sensor
vertical home
sensor
■ Make sure that the reagent arm is in low position in the wash tower before moving the
sample arm.
■ Make sure that the sample arm is in its upper position (vertical home position) before
moving the reagent arm.
■ Make sure that the sample and reagent arms are in their upper positions (vertical home
position) before moving any tray.
If the Rack Used Segment In Position light (A) stays red, it is possible to adjust the switch
position as follows:
Loosen the 2 CHC screws maintaining the switch, then adjust it. The switch must be
activated when the unload rack is in position and deactivated when the rack is not in position.
■ Put your finger on the "rack used segment full" sensor and press Read Sensor State.
■ Make sure that the Rack Used Segment Full light (B) becomes green.
The "rack used segment full" sensor depends on the "rack used segment in position" sensor.
If the unload rack is not in position, the Rack Used Segment Full light stays red.
■ The "new segment available" sensor is located on the load rack to check the presence of a new
segment.
■ Refer to the beam impact on the two cuvette segment extreme positions.
■ Using the 2 CHC screws maintaining its support plate (A), adjust the angle of the "new segment
available" sensor. The impact points of the beam have to be symmetric regarding to the edge of the
cuvette placed in the extreme positions (B).
A B
Cuvette
L1 ~
~ L2
L1 L2
Beam
■ Thecuvette changer vertical motions home sensor is located as shown on the following picture and is
not adjustable. The cuvette changer doesn’t stay in vertical home position (light is red).
No check available.
It is possible to adjust the "handling cover cuvette segment closed" sensor by unscrewing
the 2 CHC screws maintaining its support plate.
It is possible to adjust the "main cover closed" sensor by unscrewing the 2 CHC screws
maintaining its support plate.
■ No adjustment available.
See RAS385: Arms, 8. Shock detection
check, page 59.
■ No check available.
■ In
Services > Diagnostics > Sensors, the Lamp Power Full light must be green.
That means the lamp is functioning properly.
■ In
Services > Diagnostics > Sensors, the Power Correct light must be green.
That means the power supply is functioning properly.
Concerns
Syringe block assembly dismantling (reagent or sample)
Syringe block assembly mounting (reagent or sample)
Required tools
Hexagonal keys
Required products
Distilled water
Intervention time
0 h 15
Frequency
On request
D D
D D
■ Before reinstalling the glass barrel, pump distilled water several times and ensure that the
glass barrel is filled with water and no air bubbles are visible in the syringe.
■ Be very careful to correctly stretch the syringe cables again and replace them correctly on
the adhesive holder.
Concerns
Pumps dismantling
Pumps replacement
Water pump pressure check
Required tools
Hexagonal keys
Flat screwdriver
Phillips screwdriver
TOOL, BARFLEX (PRESS. 0-10BARS) MAM013AS
(1207899013)
Required products
None
Intervention time
1 h 00
Frequency
On request
1. Pumps dismantling
■ Switch the instrument off and disconnect the power supply cable.
■ Remove the covers (see RAS377: Covers dismantling, page 1):
Remove the loader cover, the cuvettes hatch, the connection hatch and the cuvettes cover.
water pump
waste pump
waste pump
black connector
■ Disconnect the water pump connector P56
(P56) at the rear of the instrument.
■ Disconnect the waste pump connectors
(black and red wires).
P55
Specific ABX Pentra 400 V1
■ Disconnect the water pump connector (P56)
at the rear of the instrument.
■ Disconnect the waste pump connector
(P55).
P56
2. Pumps replacement
The waste and water pumps are factory adjusted and do not require further adjustment.
The waste and water pumps are both provided with the pump support which is compatible with the old
references of waste and water pumps.
Please refer to the picture below to fasten the waste and water pumps to their dedicated
location on the pump support.
Not used
■ Stick the conductive fabric on the pump support (both provided in the kit).
15 mm
conductive fabric
IN
OUT
OUT
It might be necessary to cut the tubings to ensure a better connection with the fittings of the
new pump.
waste pump
black connector
P55
■ Connect the power supply cable and switch the instrument on.
■ Fill
up the hydraulic circuit as follows:
B A
- Go to Services > Customer Services >
Cycles.
- Reconnect the water tank, press Filling up
(A) and press OK.
- Then, press Priming Cycle (B) and make
sure that there is no leak.
■ Perform the water pump flow check. See RAS378: 6 month maintenance, 10. To check the sample
needle throughput, page 8.
■ Perform the pressure sensors (reagent and sample) calibration. See RAS442: Pressure sensors, 3.3.
To calibrate the pressure sensors, page 7.
■ Follow the "Check up after intervention" procedure. See RAS393: Check up after intervention, page 1.
Pressure sensors
Concerns
To replace the pressure sensors and board
To adjust the pressure board voltage
Pressure sensors activation, configuration, calibration
Required tools
Hexagonal keys
Flat screwdriver
KIT, ANTISTATIC KIT MZZ015A (1207921015)
Voltmeter
Required products
None
Intervention time
1 h 00
Frequency
On request
For instruments with a serial number lower than P4-4064 / C4-0305, if you need to replace
the pressure sensors or the pressure board, you will have to replace both the pressure
sensors and board for compatibility reasons.
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
1. Switch the instrument off and disconnect the power supply cable.
J2 J1
J3
Make sure that the new pressure sensors are positioned correctly. The red square on the
pressure sensor must be in front of the white square on the syringe block support.
1. Connect the power supply cable and switch the instrument on.
2. Remove the rear plate by unscrewing the four CHC screws.
Ground
TP3
R16
8. Select the Reagent radio button (C) and follow the same procedure as for the sample syringe.
9. Make sure that the results of the factor A are between 2500 and 3900, and make sure that the
difference between the 3 results of the factor A is not > 500.
Concerns
Computer model check
Windows master CD-ROM burning procedure
Windows master installation
Required tools
None
Required products
None
Intervention time
1 h 00
Frequency
On request
■ The Windows master must be used only in case of stability problems with Windows or to
make functional new specifications.
■ This procedure will erase the data on drive C:\ or on drives C:\ and D:\ (instrument software
and customer data will be deleted).
■ Then, you will have to install the software version (RAS517: Software version installation)
and the reagent applications (RAS518: Reagent applications installation).
As several computer models are available, a label, stuck on the rear plate, allows you to identify the
computer model.
This label can be read from the optic hatch opening with the help of a flashlight, without
dismantling the computer assembly first.
The table below indicates the Windows master to be used depending on the computer model.
Windows master
Computer assembly since instrument serial #1
Ref. Version2
CCC014A->F N/A NAJ047C (1207953047) 2005/12/20
CCC014G->H P4-0853 NAJ047D (1207954047) August 2007
CCC014J P4-2166 NAJ047D (1207954047) August 2007
CCC014K P4-2349 NAJ119A (1207951119) July 2011
CCC014L P4-3214 NAJ119A (1207951119) July 2011
CCC014M P4-3391 NAJ119B (1207952119) V1.0.0
CCC014N P4-4000 / C4-0110 NAJ119B (1207952119) V1.0.0
1300013734 P4-4072 / C4-0473 1300021186 V1.0.0.6
1
Please note that the computer assembly may have been changed on the instrument. In this case, do
not take into account the instrument serial # mentioned above.
2
How to know the Windows master version you have on your instrument? Open the C:\ghost.ini file.
The Windows masters for ABX Pentra 400 and Pentra C400 are available for download. The files to be
downloaded have a *.zip extension and are named "Master_P400_PC400_V_1.0.0.6" for example.
1. Download the Windows master version you need depending on the computer model of the
instrument.
2. Save the *.zip file on your laptop (do not save it on the instrument).
3. Insert a blank USB flash drive (4 GB minimum) into a USB port.
4. Press the Windows Start button and launch the cmd.exe file.
5. Enter "diskpart" and press Enter.
6. Enter "list disk" and press Enter to list the disks available on your laptop.
7. Select the blank USB flash drive (enter "select disk 1" for example) and press Enter.
Be careful to select the blank USB flash drive and not to select another disk because you will
erase all data on the selected disk.
1. Insert the Windows master USB flash drive into a USB port.
To authorize the computer to boot on the USB flash drive, modify the System Boot into the BIOS as
follows:
2. Switch the instrument on and press DEL when the following message appears: "Press DEL to run
setup".
3. When the BIOS window appears, enter in the Boot menu.
4. Select Hard Drive BBS Priorities and press Enter.
Boot Menu
9. Press ESC and check the boot order:
- Boot Option #1 [USB flash drive name]
- Boot Option #2 [Disabled]
10. Press F4 to save modifications and choose YES to restart the computer.
The computer automatically boots on the USB flash drive.
To cancel, press Q with the AZERTY keyboard and press A with the QWERTY keyboard.
The left Shift key used to skip the automatic logon is no more functional under Windows 7.
Press CTRL+ALT+DEL keys to logoff and change current user.
The following printer drivers are pre-installed but not loaded in Windows 7 after performing the master
procedure.
These models are the ones supplied by HORIBA Medical over the past years until now:
■ OKI B4600
■ Epson M2000
■ Epson M2400
■ Epson 6200
■ Epson WP4015
■ Epson WF5110
To install a printer:
1. Open the Windows menu, click on Devices and Printers.
2. Connect one of these printers only by USB cable, and power on the printer.
The drivers will be loaded after 1 minute.
3. Enter Control Panel > Hardware and Sound > Devices and Printers.
4. You must see your printer model appearing in the Printers and Faxes list.
For the printer models listed above, printing operations have been tested and fully validated.
Other printer models can be connected but HORIBA Medical cannot guarantee correct
printing operations on all the printer models.
4. Press OK.
5. Touch each of the four corners of the screen to calibrate the touchscreen.
6. Press Apply, then OK.
The Windows masters for ABX Pentra 400 and Pentra C400 are available for download. The files to be
downloaded have an *.iso extension and are named "Master_P400_PC400_V_1.0.0" for example.
■ Download the Windows master version you need depending on the computer model of the instrument.
■ Save the *.iso file on your laptop (do not save it on the instrument).
■ Insert a blank CD-ROM in the CD writer.
■ Start the CD burning software.
■ Burn the ISO image to the CD-ROM.
It is seriously recommended to wait one minute between the switch off and the switch on of
the instrument, to prevent any damage to the power supply.
Option (1): erases the data on drive C:\; installs Windows on drive C:\.
Option (2): erases the data on drives C:\ and D:\; installs Windows on drive C:\ and creates a
Backup folder on drive D:\.
Option (Q): enables to quit the program.
Concerns
Software version downloading
Software version installation
Required tools
None
Required products
None
Intervention time
0 h 15
Frequency
On request
■ If Full installation is selected when installing the software version, the complete
configuration (applications, calibrators, controls, settings, etc.) will be lost.
Then, you have to install the reagent applications again. See RAS518: Reagent applications
installation, page 1.
■ If Update is selected, you will not lose the configuration (applications, calibrators, controls,
settings, etc.) neither the patient results.
■ Press Next.
■ Press Install.
■ The instrument will ask you: "Ready to Install?", press Yes.
■ The Eprom will be updated automatically and then the software as well (it will take a few minutes).
If Full installation is selected, the following message will appear during the update:
"The directory: "C:\Program Files\P400 Software\" already exists.
Continue the task: "Download P400 Eprom", "Create a desktop icon", "Full installation"?".
Press Yes.
Concerns
Reagent applications downloading
Reagent applications installation
Required tools
None
Required products
None
Intervention time
0 h 15
Frequency
On request
■ Install your reagent applications support (CD-ROM or USB flash drive) on the instrument.
■ Select the support type in the dialog box and press OK.
The applications for which an update is available on your support are listed in two tables: one for major
parameter updates, another for minor parameter updates.
■ When a major parameter is updated in an application, the current calibration for this test is lost. A new
calibration must be performed. If the number of calibrator levels or the calibration predilution is
modified, the calibrator target values for this test are also deleted and must be reconfigured.
■ When a minor parameter is updated in an application, the current calibration for this test is kept in
memory. A new calibration is not required.
For detailed information concerning major and minor parameters, refer to the ABX Pentra 400 user
manual.
Each table indicates the application code, the current application version number and modification date
and time, the update application version number, if the application is selected to be updated.
■ Press Edit.
■ By default, all applications are selected to be updated. If necessary, deselect the applications that
should not be updated.
If an application is already present on the instrument with the same test name, the same
application code or the same application local code but a different channel number, then the
application is unselected by default and cannot be updated. The following message is
displayed: "At least one application has the same name or code with different channel in the
media." In this case, the test name, the application code or the application local code must
be modified before updating this application.
■ Press OK to validate.
When an update of the reagent online help is available on your support and at least one application is
unselected, a dialog box informs the user that the whole reagent online help is going to be updated
whereas at least one application will not be updated.
■ Press OK to validate.
■ Press Cancel to cancel the applications update.
■ Install your reagent applications support (CD-ROM or USB flash drive) on the instrument.
■ Select the support type in the dialog box and press OK.
The applications for which an update is available on your support are listed in two tables: one for major
parameter updates, another for minor parameter updates.
■ When a major parameter is updated in an application, the current calibration for this test is lost. A new
calibration must be performed. If the number of calibrator levels or the calibration predilution is
modified, the calibrator target values for this test are also deleted and must be reconfigured.
■ When a minor parameter is updated in an application, the current calibration for this test is kept in
memory. A new calibration is not required.
For detailed information concerning major and minor parameters, refer to the Pentra C400 user manual.
Each table indicates the application code, the current application version number and modification date
and time, the update application version number, if the application is selected to be updated.
■ Press Edit.
■ By default, all applications are selected to be updated. If necessary, deselect the applications that
should not be updated.
If an application is already present on the instrument with the same test name, the same
application code or the same application local code but a different channel number, then the
application is unselected by default and cannot be updated. The following message is
displayed: "At least one application has the same name or code with different channel in the
media." In this case, the test name, the application code or the application local code must
be modified before updating this application.
■ Press OK to validate.
Modification of the following method parameters could affect the ratio consistency:
■ pre-dilution parameters (diluent solution, factor, delay)
■ cleaning parameters
■ analysis cycles parameters
The following modifications always affect the ratio consistency:
■ modification of the specimen type in the method parameters
■ modification of the basic unit
■ creation of an incompatibility for the methods used in the same ratio
For detailed information, refer to the "Settings > Application Configuration" chapter of the
Pentra C400 user manual.
- If an application is linked to a profile and the sample type is modified in this application, the
application cannot be updated. In this case, the profile must be deleted before updating the
applications.
- If a reagent is already present on the instrument with the same reagent short name but a different
reagent number, the reagent cannot be updated. In this case, the reagent short name must be modified
before updating the applications.
- If the container type for a solution with a reagent number between 600 and 799 is changed, a dialog
box informs the user that the solution will be deleted from the Reagent Configuration menu.
■ Press OK to validate. In this case, after the applications update, the container type must be
reconfigured in Services > Application Configuration > Reagents and the solution in the
Reagent Configuration menu.
■ Press Cancel to cancel the applications update.
- When an update of the reagent online help is available on your support and at least one application
is unselected, a dialog box informs the user that the whole reagent online help is going to be updated
whereas at least one application will not be updated.
■ Press OK to validate.
■ Press Cancel to cancel the applications update.
Printer installation
Concerns
Overview
Printer installation
Preliminary
Driver installation for EPSON WF-5110DW printer (for
example)
Printer selection
Printer properties setup
Printer connection
Required tools
Driver delivered with the printer
Required products
One of the listed printers
Intervention time
0 h 20
Frequency
On request
1. Overview
2. Printer installation
2.1. Preliminary
From the instrument application (Services > System Configuration > Printer), make sure that the
printer is listed.
■ If it is, go directly to 2.3. Printer selection, page 5
■ If not, go to 2.2. Driver installation for EPSON WF-5110DW printer (for example), page 2
In order to install an EPSON WF-5110DW printer on your instrument, you need to perform the following
steps.
■ Copy the driver to a USB flash drive.
■ Go to Services > System Configuration > Printer.
■ Press Edit and then Add Printer.
■ Click Next.
■ Insert
your USB flash drive and click
Browse.
After installing your printer, check if it is set as default. To do that, you need to perform the following
steps.
■ Go to Services > System Configuration > Printer.
■ Press Edit.
■ From the Printer List, select the printer you want to set as default.
■ Press Set Default Printer.
■ Press OK to validate.
■ Select:
- Paper Source: Auto Select
- Document Size: A4
- Paper Type: Plain paper
- Color: Grayscale
■ Click OK.
■ Press OK to validate.
Please note that a USB cable, ref. DAC051A (1201891051), is delivered with the instrument
in order to connect the printer to the instrument.
In addition, a US power cable, ref. DAC012A (1201891012), is also delivered with the
instrument for the printer connection (only for US).
Concerns
To install the barcode reader
Barcode reader default configuration
To set up the barcode reader
To test the barcode reading
Required tools
None
Required products
None
Intervention time
0 h 20
Frequency
On request
The barcode reader has been set up so that it can read the following types of barcodes:
■ ITF 2/5 (2 of 5 interleaved) without check digit (16 characters max.)
■ Code 39 without check digit (16 characters max.)
■ Code 128 (99 characters max.)
■ Codabar (16 characters max.)
This default configuration has been already done on the barcode reader. However, if you need to reset
the barcode reader to the default configuration, you can follow the default configuration procedure (see
below).
KBD-AT-ALT
I 2 of 5 Set Length
1. If the ITF 2/5 with check digit is used in the laboratory, you must set up the barcode reader as follows.
2. To reset the barcode reader to the ITF 2/5 without check digit configuration (see below).
1. If the Code 39 with check digit is used in the laboratory, you must set up the barcode reader as
follows.
2. To reset the barcode reader to the Code 39 without check digit configuration (see below).
1224488 121314151617
4.2. Code 39
12345ABCDE
Barcode checksum: No
4.4. Codabar
Barcode checksum: No
37859 123456/$
Cooling unit
Concerns
Cooling unit dismantling
Cooling unit parts replacement
Air fan replacement
Float switch replacement
Control board replacement
Pump replacement (for CU401 only)
Bleed screw O-ring replacement (for CU401 only)
Required tools
Hexagonal keys
Phillips screwdriver
Open-end wrench
Pliers
KIT, ANTISTATIC KIT MZZ015A (1207921015)
Required products
None
Intervention time
N/A
Frequency
On request
To avoid any damage (compressor oil into the condenser), do not tilt the cooling unit during
this operation.
Remove the reagents from the reagent tray and place them in a refrigerated area.
■ Switch the cooling unit off and disconnect the power supply cable.
To avoid anything falling into the tank, put the lid on the hole.
A A
■ Unscrew the 2 cruciform screws and
washers at the top side of the unit (A). Then,
fold away the front cover towards the front C
(B). C
■ Remove the rubber corners (C). B
■ First, perform the cooling unit dismantling procedure. See 1. Cooling unit dismantling, page 2.
Ensure that the air fan is positioned in the correct direction: the sticker must be visible.
■ To simplify the air fan reassembling, it is better to fasten the right screw first (when you are
in front of the air fan with sticker visible).
■ In case the connectors are too loose, remove them and tighten them a little bit more with pliers.
■ Only fix the sheath and the ground wire with the Ty-Raps™, do not take the 2 power supply
wires.
A
C
■ Unscrew the 3 screws and washers using an 7-mm open-end wrench and remove the air fan.
Ensure that the air fan is positioned in the correct direction: the sticker must be visible.
Sticker
■ First, perform the cooling unit dismantling procedure. See 1. Cooling unit dismantling, page 2.
C1
GR1
R2
REL1
R1
R3
R4
T1
D2
RC1
TR1
■ On the control board, disconnect the float
switch cable from the SU6 connector.
SK2
S11
SSR1
SK1 SK3 SK4 SK5 SU6
SSR1
S11
■ On the control board, lift up and disconnect
SK2
the float switch cable from the SU6
connector.
TR1
T1
D2
RC1
R1
R3
R4
REL1
R2
GR1
C1
As the electronic devices are very sensitive to electrostatic discharges (ESD), the use of an
antistatic kit is mandatory during boards handling/dismantling.
R2
REL1
R1
R3
R4
D2
T1
RC1
TR1
To instrument
connector
SK2
S11
SSR1
To compressor
To float switch
To float switch
SSR1
To compressor
S11
SK2
To instrument
TR1
connector
RC1
T1
D2
R4
R3
R1
REL1
R2
GR1
C1
■ First, drain the cooling unit. See RAS379: Yearly maintenance, 2. Cooling unit, page 7.
■ Perform the CU401 cooling unit dismantling procedure. See 1. Cooling unit dismantling, page 2.
Pay attention not to lose the 2 blue washers located at the back of the IN/OUT plate screws.
SSR1
S11
■ On the control board, disconnect the float
SK2
switch cable from the SU6 connector and
the pump cable on the SK4 connector.
TR1
T1
D2
RC1
R1
R3
R4
REL1
R2
GR1
C1
B B
■ On the pump:
- Disconnect the ground wire (A).
- Unscrew the 4 cruciform screws and
washers (one with a ground wire) (B).
A
B B
■ Slightly
lift the pump up and towards the
back to access the tubings.
■ Cutand remove the 2 collars. Then,
disconnect the tubings.
To reconnect the tubings, use the 2 collars provided with the pump.
■ Put the collar on the tubing and plug the tubing into the connector.
■ Then, with pliers, tighten both sides of the square part of the collar.
■ First, drain the cooling unit. See RAS379: Yearly maintenance, 2. Cooling unit, page 7.
bleed screw
collar