I Smart 30 Manual
I Smart 30 Manual
Contents
1 Introduction
Safety .......................................................................................................... 1-1
Symbols and Terms................................................................................................ 1-3
Product Description ............................................................................................. 1-5
2 Installation
Installation Requirement ..................................................................................... 2-1
Start-Up ................................................................................................................ 2-2
Printer Paper ........................................................................................................ 2-6
Cartridge ................................................................................................. 2-8
3 Instrument Settings
Screen Menus ....................................................................................................... 3-1
Sample Setup ..................................................................................................... 3-10
QC Setup ........................................................................................................... 3-16
Instrument Setup ............................................................................................... 3-18
Print Setup ......................................................................................................... 3-23
Interface Setup ................................................................................................... 3-25
4 Sample Analysis
Patient Samples ................................................................................................... 4-1
QC Samples ......................................................................................................... 4-6
5 Database
Patient Data..................................................................................................... 5-1
QC Data ............................................................................................................... 5-4
Calibration Data ................................................................................................... 5-8
Cartridge Data ................................................................................................... 5-10
1. Introduction
6 Shutdown
Analyzer Shutdown ............................................................................................. 6-1
Power Recovery ................................................................................................... 6-3
Data Recovery ................................................................................................ 6-5
7 Maintenance
Calibration............................................................................................................ 7-1
Cartridge Removal ............................................................................................... 7-3
Analyzer Information ...................................................................................................7-5
Analyzer Status ................................................................................................... 7-7
Cleaning ............................................................................................................... 7-8
8 Troubleshooting
Trouble Shooting ................................................................................................ 8-1
Error Code ........................................................................................................... 8-5
9 Specifications
Operating Specifications ..................................................................................9-1
Instrument Specifications .................................................................................... 9-2
Cartridge Specifications ....................................................................................... 9-3
Principles ..................................................................................................... 9-4
Performance .................................................................................................... 9-6
Appendices
Appendix A: Sample Collection and Handling ............................................... 10-1
Appendix B: Order Information ....................................................................... 10-3
Appendix C: Warranty .......................................................................................... 10-4
1. Introduction
1. Introduction
Safety
General Use only the provided power cord and adapter.
Warnings Do not use damaged power cord, adapter, or loose outlet.
Never touch the power supply accessories with wet hands.
Keep dust away from the outlet and power cord.
Do not use or store any hot equipment or flammable
material near the analyzer or power supply accessories.
Do not allow water or foreign substances to get into the
analyzer or power supply accessories.
Do not directly look at the red light emitting from the
barcode scanner as direct eye exposure to this light can
damage vision.
Safety, continued
Biohazard All materials used in collecting blood from animals should
Caution be treated as biohazardous materials with the potential
carrying infectious agents capable of producing disease.
All biohazardous materials should be handled and disposed
of in accordance with applicable rules and regulations of the
hospital, laboratory, or other testing facility.
Wear appropriate personal protective clothing (lab coat,
gloves, goggles, etc.) before operating the analyzer.
Be careful not to let the sample and/or collecting tools
directly touch the mouth, eyes, mucus membranes, or any
area with broken skin.
Wash hands after collecting the sample or using the
analyzer.
CE mark
FCC mark
Batch code
Use by
Biological risk
Electrical and electronic equipment waste
that requires specific disposal instructions
from the manufacturer
Printer
DC power port
Off (power)
On (power)
K+ Potassium ion
Cal Calibration
Product Description
Intended Use The i-Smart 30 VET electrolyte analyzer is intended to be used
for the measurements of sodium, potassium, and chloride in
whole blood, plasma, or serum. The analyzer is used by
laboratory professionals for in vitro veterinary diagnostic
testing.
Analyzer
Touch
screen
Sampler Cartridge
cover door
Printer
Handle
Power Vent
switch
Power port
USB ports
LAN port
Serial port
Cartridge
cover
Accessories
Analyzer base
2. Installation
Installation Requirement
Unpacking Inspect the shipping package of the product for any signs of
damage from shipment.
Ensure all listed components are included in the package.
Note:
The analyzer should be installed on a horizontal, stable
surface in a well-ventilated area without direct sunlight or
heat.
Allow enough space for the cartridge door of the analyzer
to open.
Allow at least 10 cm of space from the back of the analyzer
for adequate ventilation.
Start-up
Caution Check that the power switch is in “ ” (OFF) position.
Always connect the power according to the steps described
in this manual.
Always use a grounded electrical outlet.
Use only the power cord and power adapter provided by the
manufacture.
Electrical plugs and sockets vary by countries. If necessary,
use appropriate power plug or power strips to connect the
provided power cord to the outlet.
Power 1. Plug the power cord into the socket of the power adapter.
Connection
2. Plug the power adapter into the power port on the back of
the analyzer.
Start-up, continued
Barcode 1. Insert the USB connector of the barcode scanner into a USB
Scanner port on the back or side of the analyzer.
Connection
Note:
When the analyzer is turned on, the barcode scanner will
make a beep sound and the indicator light on the scanner
will turn on briefly.
Start-up, continued
Turn On 1. Facing the back of the analyzer, flip the black power switch
on the lower left side, marked “ ” to the “ ” position.
2. The screen will turn on and the rebooting will start.
Start-up, continued
Turn On, 5. Check that the power cord icon appears at the bottom
continued row of the screen.
Note:
If the power cord icon does not appear on the screen and
the battery icon appears instead, it indicates that the
analyzer is on battery power. Check for any loose power
connections between the analyzer and the electrical outlet.
If no loose power connection is found and the power cord
icon still does not appear, call a service engineer
immediately.
Printer Paper
Install Paper 1. Facing the back of the analyzer, flip down the printer cover.
2. Insert the end of the paper in parallel with the printer slot.
The printer will begin to feed the paper automatically.
Note:
The cut end of the paper should be straight and clean for
auto feeding.
Paper should be fed from the bottom of the roll.
Remove Paper 1. Facing the back of the analyzer, flip down the printer cover
and remove the remaining paper roll.
Note:
Do not use force to pull out the paper from the printer.
Never pull the paper in the reverse direction of printing.
Cartridge
Install 1. Take out the cartridge from the cartridge box.
Cartridge 2. Press down the cover lock and remove the cartridge cover.
Cartridge, continued
Install 5. When the Scan new cartrdige barcode message appears,
Cartridge, scan the barcode on the new cartridge using the barcode
continued scanner.
6. If the analyzer accepts the barcode, the grey box will turn to
green.
7. When the Insert scanned cartridge and close door message
appears, open the cartridge door.
Cartridge, continued
Install 9. Hold the cartridge door lock with two fingers and close the
Cartridge, door. If the door is properly locked, it will make a
continued clicking sound.
Note:
Never re-install the cartridge cover back to the cartridge if
the cartridge has been inserted into the analyzer. It will
cause the calibration solutions to leak in the cartridge.
Once the cartridge cover is removed, be careful with
exposed sharp edges of the cartridge parts.
3. Instrument Settings
Screen Menus
Ready Screen
No. Description
① Menu button
② Current status of the analyzer
③ Remaining test number of the installed cartridge
④ Remaining uselife days of the installed cartridge
⑩ Sound volume:
Pressing once will display volume increase/decrease icons.
⑬ Animal species:
Pressing twice quickly will display the entered reference range.
Save setup
Begin to search
Go to
a selected QC results screen
Go to
previous or next results screen
Move
highlight bar up or down
Run a QC sample
Scan QC barcode
Go to service mode
Alphabetic Keyboard
Voice Guide Besides displaying messages, the analyzer will play sound
playbacks to help the operator when performing one of
following tasks:
Blood sample introduction
QC sample introduction
Cartridge removal
Cartridge installation
Cartridge data copy
Alarm: “The battery is low”
Sample Setup
Reference 1. Go to Menu > Full Menu > Setup > 1 Sample Setup.
Ranges
2. Select 1 Reference Ranges. The following screen will
appear.
4. Press each of boxes and enter low and high limits of the
reference range for each analyte.
Note:
Before saving the setup, the analyzer will check that the
entered values meet following conditions:
- The values for low and high limits are entered.
- The low limit value is lower than the high limit value.
If any of the entered values is not valid, the analyzer will
not save the setup and ask the operator to correct the invalid
value at the setup screen.
Note:
The acceptable values for slope and offset of correlation
factors for each analyte are as following:
Analytes Slope Offset
Na+ 0.70 ~ 1.30 ±10.00
K+ 0.70 ~ 1.30 ±1.00
Cl- 0.70 ~ 1.30 ±10.00
QC Setup
QC Lot Setup 1. Go to Menu > Full Menu > Setup > 2 QC Setup. The
following screen will appear.
QC Setup, continued
QC Lot Setup, 4. For other QC materials, manually enter QC lot information
continued using the keyboard.
Instrument Setup
Date &Time 1. Go to Menu > Full Menu > Setup > 3 Instrument Setup.
2. Select 1 Date & Time. The following screen will appear.
3. Press Date Format Box and select the desired date format
from the drop-down list.
4. Press Time Format Box and select the desired time format
from the drop-down list.
5. Press Date Setup Box and enter the desired date using the
keyboard.
Note:
Instrument name will appear on the main screen and on
printouts.
Print Setup
Print Option 1. Go to Menu > Full Menu > Setup > 4 Print Setup.
2. Select 1 Print Option. The following screen will appear.
3. Press a desired Line Box and enter title using the keyboard.
Interface Setup
Option Setup Note:
Make sure that network cable(s) is appropriately connected
to the analyzer before starting interface setup.
2. Press Baud Rate Box and select the desired option from the
drop-down list. Default is 9600.
Note:
Manual setup is recommended instead of auto setup since
auto setup may cause network collision.
4. Sample Analysis
Patient Samples
Introducing Note:
Sample Sample analysis is available only when the analyzer is in
Ready status. While the analyzer is not in Ready status, the
sampler cover is locked.
Note:
To cancel a patient sample, lower the sampler cover to the
original position before pressing Aspirate.
Once Aspirate is pressed, the sample analysis cannot be
cancelled.
Note:
Be careful not to introduce air bubbles, clots, or foreign
substances along with sample to the analyzer.
5. For a capillary sample, lift the sampler cover up all the way.
Carefully insert the capillary into the septum.
Note:
Do not allow any gap between the capillary and the septum
to avoid air flow in with the sample.
Note:
If a result is within the reference range, the result will
appear in blue color.
If a result is above reference range, the result will appear in
red color along with ↑.
If a result is below reference range, the result will appear in
red color along with ↓.
Note:
The arrows on the screen will be printed as [H] or [L] on
printouts.
8. If the analyzer has been set to auto print, the analyzer will
print the results as soon as they are reported.
9. Press Exit to save the results and exit to main screen.
10. The analyzer will go through Rinse and Cal 1 process
before returning to the Ready status for a next sample.
QC Samples
Introducing 1. Press Menu and select Run QC. The following screen
QC Sample will appear.
Note:
The Run QC menu will be available only when the QC
Lot(s) has been setup at QC Setup menu.
QC Samples, continued
Introducing 4. When “Introduce QC Sample now” message appears,
QC sample, immerse the end of the sampler probe into the QC sample
continued and press Aspirate.
Note:
To cancel QC sample, lower the sampler cover to the
original position before pressing Aspirate.
Once Aspirate is pressed, the sample cannot be cancelled.
QC Samples, continued
QC Results 1. If the QC sample analysis is completed, the results will
appear along with the entered QC ranges.
Note:
If a result is within the QC range, the result will appear in
blue color.
If a result is above the QC range, the result will appear in
red color along with ↑.
If a result is below the QC range, the result will appear in
red color along with ↓.
QC Samples, continued
QC Results, 3. To transmit the results to the network, press Send.
continued 4. Press Print to print out the results. A printout similar to
following will be printed.
Note:
The arrows on the screen will be printed as [H] or [L] on
printouts.
5. Database
Patient Data
Last Patient 1. Go to Menu > Full Menu > Database > 1 Patient Data.
Results 2. Select 1 Last Patient Results. The following screen will
appear.
Note:
The same screen can be accessed through Menu > Last
Patient Results.
Patient Results 1. Go to Menu > Full Menu > Database > 1 Patient Data.
List 2. Select 2 Patient Results List. The following screen will
appear.
Note:
Search criteria for patient results are as following:
Measured date(s)
Animal species
Sample No.
Patient ID
Patient Name
QC Data
Last QC 1. Go to Menu > Full Menu > Database > 2 QC Data.
2. Select 1 Last QC Results. The following screen will
appear.
QC Data, continued
QC Results 4. To view a QC Results screen, select a desired row from the
List, list and press View. The corresponding QC results screen
continued will appear.
QC Data, continued
QC Results 1. Go to Menu > Full Menu > Database > 2 QC Data.
Search 2. Select 3 QC Results Search. The following screen will
appear.
Note:
Search criteria for QC results are as following:
Measured date (s)
QC Level
QC Lot No.
Either Pass or Fail QC results only
QC Data, continued
QC Statistics 1. Go to Menu > Full Menu > Database > 2 QC Data.
2. Select 4 QC Statistics. The following screen will appear.
Calibration Data
Calibration 1. Go to Menu > Full Menu > Database > 3 Calibration
List Data.
2. Select 1 Calibration List. The following screen will
appear.
Cartridge Data
Cartridge Data 1. Go to Menu > Full Menu > Database > 4 Cartridge Data.
Copy The following screen will appear.
6. Shutdown
Analyzer Shutdown
Caution The power of the analyzer should be turned off according to
the shutdown procedure as described in this manual. Failure
to follow the proper shutdown procedure can cause damage
to the data or the component of the analyzer.
To disconnect the power cables from the analyzer, first
unplug the power cord from the outlet. Then unplug the
adapter from the analyzer.
The cartridge cannot be removed during the shutdown
process or when the analyzer is turned off.
Power Recovery
Cartridge If the power went out while the cartridge was in use on the
Restoration analyzer, upon power recovery the cartridge can be restored
back to use, only if:
- The power interruption has been less than 24 hours and
the analyzer had been in ready status or in calibration
process when the power went out.
- The power interruption has been less than 20 minutes
and the analyzer had been analyzing a sample when the
power went out.
The maximum number that each cartridge can be restored
upon power recovery is limited to five.
Power 1. If the power has come back within the time limits that the
Recovery cartridge can be restored, the warming-up screen will
Warming-up appear.
2. At the warming-up screen, the message with the previous
power shutdown information will appear.
Data Recovery
Data Whenever the analyzer is turned on, the analyzer will check
Corruption for corrupted data that may exist in database or cartridge
Check data folder.
As long as corrupted data is not found, the analyzer will
continue to reboot.
If corrupted data is found, the analyzer will alert the
operator to initiate data recovery process to repair the
corrupted data.
Data Recovery 1. If data corruption is found, the following screen will appear.
Procedure
Note:
Upon the operator’s permission, the analyzer will carry out
data recovery process during which following action will be
taken:
In database:
- If corrupted data is found, the entire database will be
erased.
- If corrupted data is not found, the database will be fully
recovered.
7. Maintenance
Calibration
Run Cal 1. Go to Menu > Full Menu > Maintenance > 1 Run Cal.
The following screen will appear.
Note:
The same screen can be accessed through Menu > Run Cal.
Cal 2 If a sensor has failed in the previous Cal 2, the analyzer will
Auto Repeat automatically repeat Cal 2 up to two times.
While the Cal 2 repeat is in progress, the “Cal 2 Repeat in
progress” message will appear.
If the same sensor fails in Cal 2 three times in succession,
the sensor status will appear as on the main screen.
Calibration, continued
Sensor Status 1. For each sensor, a pass or failure result from the latest Cal 2
will appear as or at the main screen.
Cartridge Removal
Caution Treat the used cartridge as biohazard material.
Before removing the used cartridge, wear appropriate
personal protective clothing to protect from biohazard
materials.
Note:
The same screen can be accessed through Menu > Remove
Cartridge.
The analyzer will automatically change to the Remove the
cartridge screen in one of following situations:
The uselife of the cartridge has expired.
All tests of the cartridge have been used up.
The analyzer has been without power for more than the
allowable time limit to restore the cartridge.
Analyzer Information
Cartridge 1. Go to Menu > Full Menu > Maintenance > 3 View Info.
Information 2. Select 1 Cartridge Info. The following screen will appear.
Instrument 1. Go to Menu > Full Menu > Maintenance > 3 View Info.
Information 2. Select 2 Instrument Info. The following screen will appear.
Analyzer Status
View Status 1. Go to Menu > Full Menu > Maintenance > View Status.
The following screen will appear.
Note:
If the cartridge is properly installed, Cartridge Installation
will appear as Installed, Cartridge Door as Close, and
Sampler Cover as Close.
The Service Mode is for service engineers ONLY and its
access is protected by password.
Cleaning
Caution Wear appropriate personal protective clothing to prevent
infection when cleaning.
Clean the analyzer after use or periodically.
Do not spray cleaning solution directly onto the analyzer.
Do not allow cleaning solution to enter the analyzer.
Do not use force to wipe the screen.
Prepare a hypochlorite cleaning solution immediately
before use.
Dispose of all waste after cleaning in accordance with the
laboratory’s established procedures for disposing of
biohazardous materials.
8. Troubleshooting
Trouble Shooting
Instruction If the problems described below are encountered during
installation and/or operation of the analyzer, try the
suggested solutions as described in this manual.
If the problem persists, please call a service engineer for
further assistance.
Barcode When scanning barcode, the scanner does not emit the red light:
Scanner
1. Remove the USB connector of the barcode scanner from the
analyzer.
2. Insert the USB connector into the same USB port of the
analyzer. The barcode scanner will make a beep sound and
the indicator light on the scanner will turn on briefly
3. Wait 5 seconds for the analyzer to recognize the barcode
scanner.
4. If the same problem occurs, repeat the procedure from step
1 with a different USB port of the analyzer.
When scanning barcode, the scanner emits red light, but does
not take barcode (no beep sound and no indicator light on):
1. Run Cal 2.
2. If needed, repeat additional Cal 2 a few times more.
Error Code
Error Code 1. If the analyzer encounters an error while in use the
following error code will appear on the screen.
9. Specifications
Operating Specifications
Measured Measured Parameters
Parameters
Parameter Range Resolution
Na+ 20 ~ 250 mmol/L 1 mmol/L
K+ 0.5 ~ 20.0 mmol/L 0.1 mmol/L
Cl- 20 ~ 250 mmol/L 1 mmol/L
Sample types: whole blood, serum and plasma
Anticoagulant: appropriate amount of lithium heparin
Sample volume: 60 μL
Sample container: syringe or capillary tube
Sample introduction: aspiration
Measuring time: 35 seconds
Measuring temperature: 37.0 ± 0.2 °C
Measuring method : Ion Selective Electrode
Calibration : Automatic or manual
Instrument Specifications
Instrument Internal PC:1 GHz process Mobile PC / 1 GB RAM / 4 GB
Specifications Flash Memory
Operating System: Microsoft® Windows® XP Embedded
Display:7" TFT-LCD, touch screen
Printer: 2" thermal printer (internal printer)
Printer paper: thermal (width: 57 mm, diameter: 30 mm)
Port: USB (3 ports), Serial (RS-232), LAN (RJ45 Ethernet)
Power adapter:
AC-DC power supplies (IEC/EN 60950-1 approved)
input: 100 ~ 240 VAC 50/60 Hz (±10%), 150 W
output: + 24 VDC, 2.7 A, 65 W
Input power: + 24 VDC, within 65 W
Internal fuse: 125 V (AC/DC combo), 3 A (slow blow)
Internal battery: 14.8 V, 4.4 Ah (Lithium-ion cells: 4S2P)
Discharge time: maximum two hours
Charging time: maximum two hours
Battery life:
20% reduced capacity for charging/discharging for 300
times.
Replace when the capacity drops below 50%
(discharging time is less than one hour).
The life and replacement cycle of the battery can vary
depending on operating conditions.
Storage temperature : -20 ~ 50 °C
Storage humidity : 0 ~ 90% (relative humidity)
Size (HxWxD): 292 mm x 256 mm x 208 mm
Weight: 5.5 Kg
Cartridge Specifications
Cartridge Unit: 1 cartridge
Uselife: 4 weeks
Number of tests available: 30T, 50T, 100T, 150T, 200T
Shelf life: 12 months from the manufacturing date
Storage temperature: 10 ~ 30 °C
Components:
Sensors
Cal 1solution, 400 mL
Cal 2 solution, 40 mL
Reference solution, 40 mL
Sampler and waste bag
Valve and tubing
Principles
Measurement The measurements of sodium, potassium, and chloride by the i-
Principle Smart 30 VET electrolyte analyzer is based on the principle of
ion-selective electrode (ISE). In an ion-selective electrode, an
electrical potential is established across a membrane that is
selective to a specific ion.
The i-Smart 30 VET uses the ion-selective electrodes that are
composed of polymeric sensing membranes dispensed over
internal hydrogel layers on a thin plastic substrate as shown in
the figure below. The Ag/AgCl reference electrode is used and a
liquid junction is formed where the reference solution flowing
over the reference electrode meets the sample solution flowing
over the ion-selective electrodes.
The electric potential of the ion-selective electrodes measured
against the reference electrode is used to determine the activity
(a) or effective concentration (c) of the ions of interest in a
sample.
Principles, continued
Measurement RT
EEo ln(a)
Principle, nF
continued where, (+) for cation, (-) for anion
E: monitored potential Eo: potential at a = 1
R: gas constant T: temperature in Kelvin scale
n: valence of ion F: Faraday constant
a: activity of the target ion
Since the ion-selective electrodes tend to drift over the time, the
i-Smart 30 VET analyzer periodically calibrates the sensors
during the lifetime of the cartridge according to the pre-
determined two-point calibration schedule. For such two-point
calibrations, the analyzer uses two calibration solutions
provided in the cartridge. Furthermore, the analyzer carries
out one-point calibrations of the sensors using one of the
calibration solutions in order to correct drifting baseline of the
sensors between two-point calibrations.
Performance
Introduction The results obtained during evaluation of i-Smart 30 VET
electrolyte analyzers at i-SENS’ research laboratories are shown
below to demonstrate the typical performance characteristics of
the i-Smart 30 VET.
K+ QC Material Precision
Performance, continued
Whole Blood Whole blood precision was obtained using seven levels of
Precision canine whole blood. Seven levels were tested in three or four
replicates, depending on the availability of sample amount, on
six analyzers. Low or high levels were prepared by adding a
concentrated or a diluted electrolyte solution to whole blood,
respectively, to expand the tested range.
Performance, continued
Whole Blood Cl- Whole Blood Precision
Precision, Level N Per Level Mean (mmol/L) SD %CV
continued
1 24 100.8 0.38 0.4
2 24 101.2 0.41 0.4
3 24 109.5 0.51 0.5
4 18 117.1 0.42 0.4
5 18 127.4 0.78 0.6
6 18 141.4 0.92 0.7
7 18 149.7 1.28 0.9
Whole blood The data from the whole blood precision study were used to derive
Inaccuracy the whole blood inaccuracy. Reference values for sodium,
potassium, and chloride were obtained using a traditional
laboratory electrolyte analyzer. The bias results were calculated by
subtracting the mean of six analyzers from the mean of the
reference analyzer. The acceptance criteria are established from
CLIA 88.
Performance, continued
Whole blood K+ Whole Blood Inaccuracy
Inaccuracy, Mean Target Specification
continued Level N Per Level Bias
(mmol/L) (mmol/L) (mmol/L)
1 24 2.30 2.38 0.08 ± 0.5
2 24 2.97 2.97 0.00 ± 0.5
3 24 4.10 4.15 0.05 ± 0.5
4 18 4.29 4.33 0.04 ± 0.5
5 18 5.88 5.90 0.02 ± 0.5
6 18 7.81 8.03 0.22 ± 0.5
7 18 8.78 8.83 0.05 ± 0.5
Performance, continued
Whole blood The data from the whole blood precision in the previous section
Linearity were used to calculate the whole blood linearity as shown in the
following table and graphs.
Analyte N per level Slope Intercept R2 Range
Na+ 18 to 24 0.973 +6.271 0.996 122 - 175
K+ 18 to 24 0.986 +0.007 0.999 2.3 - 8.5
Cl- 18 to 24 1.047 -4.349 0.997 104 - 156
Performance, continued
Whole blood K+ Whole Blood Linearity
Linearity,
continued
Performance, continued
Aqueous The aqueous solution linearity was obtained using seven levels
Solutions of electrolyte aqueous solutions. Seven levels were tested in
Linearity four replicates on eleven i-Smart 30 VET analyzers.
The linearity data are shown in the following table and graphs.
Performance, continued
Aqueous K+ Aqueous Solution Linearity
Solutions
Linearity,
continued
Performance, continued
Interferences Following substances are known to interfere with analysis results of
i-Smart 30 VET electrolyte analyzers.
Substance Interference
Na+ heparin or
Erroneously high Na+ results
Na+ containing anticoagulants
Whole Blood Use heparinized vacuum blood collection tubes for whole
blood.
Collect blood up to the fill indicator on the tube label.
Immediately after collecting blood, roll the tube between
palms or gently shake it slowly up and down 8 to 10 times
to thoroughly mix the blood and anticoagulant.
Appendix C: Warranty
The product warranty for the analyzer and its components excluding the
cartridge is one year from the product purchase date on the VAT invoice.
Product quality assurance applies only if the product has been properly handled
and used under normal conditions and appropriately maintained according to
the operator's manual.
Please call a service engineer responsible for the product if you have any
question.