ForaCare Diamond PRIMA User manual

Blood Glucose Monitoring System
Système de contrôle de la glycémie
Owner’s Manual
Manuel de I’utilisateur
ver 2.0 2021/11 311-4281100-055
For self-testing /
Pour auto-mesure
ForaCare Suisse AG
Neugasse 55, 9000, St. Gallen, Switzerland
www.foracare.ch
0123 FORA DM10
MedNet EC-REP GmbH
Borkstraβe 10, 48163, Mϋnster, Germany

EN-1
Safety Information
Read the following Safety Information thoroughly before using
the device.
• Use this device ONLY for the intended use described in this
manual.
• Do NOT use accessories which are not specied by the
manufacturer.
• Do NOT use the device if it is not working properly or
damaged.
• This device does NOT serve as a cure for any symptoms or
diseases. The data measured is for reference only. Always
consult your doctor to have the results interpreted.
• The blood glucose test strip can NOT be used for the
testing of newborns.
• Before using this device to test blood glucose, read all
instructions thoroughly and practice the test. Carry out all
the quality control checks as directed.
• Keep the device and testing supplies away from young
children. Small items such as the battery cover, batteries,
test strips, lancets and vial caps are choking hazards.
• The use of this instrument in a dry environment, especially
if synthetic materials are present (synthetic clothing,
carpets etc.) may cause damaging static discharges that
may cause erroneous results.
• Do NOT use this instrument in close proximity to sources
of strong electromagnetic radiation, as these may interfere
with the correct operation.
• Proper maintenance as well as timely calibration of the
device together with the control solution is essential in
ensuring the longevity of your device. If you are concerned
about the accuracy of the measurement, please contact
the place of purchase or customer service representative
for assistance.
KEEP THESE INSTRUCTIONS IN A SAFE PLACE
Important Information
• Severe dehydration and excessive water loss may cause
readings which are lower than actual values. If you believe
you are suering from severe dehydration, consult a
healthcare professional immediately.
• If your blood glucose results are lower or higher than usual,
and you do not have symptoms of illness, rst repeat the
test. If you have symptoms or continue to get results higher
or lower than usual, follow the treatment advice of your
healthcare professional.
• Use only fresh whole blood sample to test your blood
glucose. Using other substances will lead to incorrect
results.
• If you are experiencing symptoms that are inconsistent
with your blood glucose test results and you have followed
all instructions described in this owner’s manual, call your
healthcare professional.
• We do not recommend using this product on severely

EN-2
Introduction
Intended Use
This system is intended for use outside the body (in vitro
diagnostic use) by people with diabetes at home and by
health- care professionals in clinical settings as an aid to
monitor the eectiveness of diabetes control. It is intended
to be used for the quantitative measurement of glucose
(sugar) in fresh capillary (from the nger, palm, forearm, and
upper arm) and venous blood samples. It should not be used
for the diagnosis of diabetes, or testing on newborns.
Professionals may test with capillary and venous blood
sample. Use only heparin for anticoagulation of whole blood.
Home use is limited to capillary blood from the nger tip and
the approved sites.
Test Principle
Your system measures the amount of sugar (glucose)
in whole blood. The glucose testing is based on the
measurement of electrical current generated by the reaction
of glucose with the reagent of the strip. The meter measures
the current, calculates the blood glucose level, and displays
the result. The strength of the current produced by the
reaction depends on the amount of glucose in the blood
sample.
For example:
1)120 mg/dL ÷ 18 = 6.6 mmol/L
2)7.2 mmol/L x 18 = 129 mg/dL approximately
hypotensive individuals or patients in shock. Readings
which are lower than actual values may occur for
individuals experiencing a hyperglycaemic-hyperosmolar
state, with or without ketosis. Please consult the healthcare
professional before use.
• The measurement unit used for indicating the
concentration of blood glucose can have mg/dL or mmol/L.
The approximate calculation rule for conversion of mg/dL
in mmol/L is:
mg/dL Divided by 18 = mmol/L
mmol/L Times 18 = mg/dL

EN-3
Product Overview
1. Test Strip Slot
4. SET Button
5. Battery Compartment
7. USB Port
8. MAIN Button
Screen Display
1.Blood Drop Symbol
8.Time
9.Day Average
10. Reminder Alarm
11. Face Low/High Symbol
12. Measurement Unit
13. Test Result
14. Low Battery Symbol
15. Test Strip Symbol
3.Ketone Warning
4.Warning Symbol
5.Memory Symbol
6.Measuring Mode
7.Date
Getting Started
Initial Setup
Please follow the initial setup procedure before using the
device for the rst time or after you have replaced the
battery. When the battery power is extremely low and“ &
”appears on the screen, the meter cannot be turned on.
Step 1: Enter the Setting Mode
Open the battery cover and press SET. The display turns on.
Step 2: Conguring the Settings (Date, Time Format,
Time, Universal Tone, Memory Deletion and Reminder
Alarm)
2.Universal Tone
2. Strip Indication Light
3. Test Strip Ejector
6. Display Screen

EN-4
Note:
• You may setup Beep On, Universal Tone On and Beep O by
press MAIN to change it.
• When Universal Tone is turned on, the meter guides you
through the blood glucose test using beep tones; it also
outputs the result as a series of beeps.
• When Beep is turned o, the alarm function will remain
eective.
• During memory deletion, select“ ”to keep all saved
results.
• You may set it up to four reminder alarms.
• To turn o an alarm, nd the alarm number by pressing
SET, then press MAIN to toggle On to OFF.
• When the alarm goes o, the device will automatically
turn on. Press MAIN to mute the alarm. If you do not press
MAIN, the device will beep for 3 minutes then switch o.
• If the device is idle for 3 minutes during the setting mode,
it will turn o automatically.
Press MAIN repeatedly to adjust the value or enable/disable
the setting. Then press SET to conrm the setting and switch
to another eld.

EN-5
Testing Your Blood Glucose
Test Strip Appearance
Absorbent Hole
Apply a drop of blood
here. The blood will be
automatically absorbed.
Conrmation Window
This is where you conrm
if enough blood has been
applied to the absorbent hole
in the strip.
Test Strip Handle
Hold this part to insert
the test strip into the slot. Contact Bars
Insert this end of the test strip
into the meter. Push it in rmly
until it will go no further.
Inserting a Test Strip
Insert the test strip into its slot.
Important!
The front side of test strip should face up when inserting the
test strip. Test results might be wrong if the contact bar is not
fully inserted into the test slot.
Important!
To reduce the chance of infection:
• Never share a lancet or a lancing device.
• Always use a new, sterile lancet. Lancets are for single use
only.
• Avoid getting hand lotion, oils, dirt, or debris in or on the
lancets and the lancing device.
Preparing the Lancing Device
1.Remove the cap.
2.Insert a new lancet rmly into the white lancet holder cup.
3.Remove the protective disk on the lancet.
Hold the lancet rmly in place and twist o the protective
disk.
4.Replace the cap until it snaps or clicks into place.
5.Rotate the dial to set the desired lancing depth.

EN-6
6.Pull the cocking control out until the orange bar appears
on the release button window.
Obtaining the Blood Sample
Please follow the suggestions below before obtaining a drop
of blood:
• Wash and dry your hands before starting.
• Select the puncture site either on your ngertips or other
body parts.
• Rub the puncture site for about 20 seconds before
penetration.
Blood from the ngertip
1.Press the lancing device tip rmly against the lower side of
your ngertip.
2.Press the release button to prick your nger. A click
indicates that the puncture is complete.
Blood from sites other than the ngertip
Alternative site testing (AST) is when individuals check their
blood glucose levels using other areas of the body other
than the ngertips. The FORA test strips allow AST to be
performed on sites other than the ngertips. Please consult
your health care professional before you begin AST.
Alternative site sample results may be dierent from ngertip
sample results when glucose levels are changing rapidly (e.g.,
after a meal, after taking insulin, or during or after exercise).
We strongly recommend that you perform AST ONLY at the
following times:
• During a pre-meal or fasting state (more than 2 hours since
the last meal).
• Two hours or more after taking insulin.
• Two hours or more after exercise.
Do NOT rely on test results at an alternative sampling site,
but use samples taken from the ngertip, if any of the
following applies:
• You think your blood sugar is low.
• You are not aware of symptoms when you become
hypoglycemic.

EN-7
• The results do not agree with the way you feel.
• After a meal.
• After exercise.
• During illness.
• During times of stress.
To obtain a blood sample from the alternative sites, please
rub the puncture site for approximately 20 seconds.
1.Replace the lancing device cap with the clear cap.
2.Pull the cocking control out until the orange bar appears
on the release button window.
Important!
• Do not use results from alternative site samples to calibrate
continuous glucose monitoring systems (CGMS), or for
insulin dose calculations.
• Choose a dierent spot each time you test. Repeated
punctures at the same spot may cause soreness and
calluses.
• Avoid lancing the areas with obvious veins to avoid
excessive bleeding.
• It is recommended to discard the rst drop of blood as it
might contain tissue uid, which may aect the test result.
Make Blood Glucose Test
1.Insert the test strip into the test slot of the device. Wait for
the device to display the test strip“ “ and blood drop
“ “.
2.Select the appropriate measuring mode by pressing MAIN.
• General Tests ( ) - any time of day without regard to
time since the last meal.
• AC ( ) - no food intake for at least 8 hours.
• PC ( ) - 2 hours after a meal.
• QC ( ) - testing with control solution.
3.Obtain a blood sample.
Use the pre-set lancing device to puncture your desired
site. After penetration, discard the rst drop of blood with a
clean tissue or cotton. Gently squeeze the punctured area to
obtain another drop of blood. Be careful NOT to smear the
blood sample. The volume of blood sample must be at least
0.5 microliter (μL) for blood glucose testing.
1
2

EN-8
Announcement of Test Result by Universal
Tone
The blood glucose results will be broken down into individual
digits and each digit represents the corresponding number
of beeps.
The result is announced three times in succession and each
time is preceded by two quick beeps. So you will hear: 2
quick beeps – results – 2 quick beeps – results – 2 quick
beeps – result.
For mg/dL meters, the hundreds are always announced, even
when the result is below 100.
Examples:
80 mg/dL is announced as 1 long beep (0) – 1 single pause –
8 single beeps (8) – 1 single pause – 1 long beep (0)
182 mg/dL is announced as 1 single beep (1) – 1 single pause
– 8 single beeps (8) – 1 single pause – 2 single beeps (2)
For mmol/L meters, the tens are always announced, even
when the result is below 10. The decimal point is represented
by 1 quick beep.
Examples:
6.0 mmol/L is announced as 1 long beep (0) – 1 single pause
– 6 single beeps (6) – 1 single pause – 1 quick beep (.) – 1
single pause – 1 long beep (0)
Note:
Information or warnings in the form of symbols displayed
together with the results are not announced acoustically.
4.Apply the blood sample.
Move your nger to meet the absorbent hole of the test
strip and the drop will be automatically be drawn onto
the test strip. Remove your nger until the conrmation
window is lled. The meter begins to count down. Do not
remove your nger until you hear a beep sound.
5.Read your result.
The results of your blood glucose test will appear after
the meter counts down to 0. The results will be stored
automatically in the meter memory.
(100 mg/dL = 5.5mmol/L)

EN-9
Disposing Used Test Strip and Lancet
To remove the used test strip, simply push the Test Strip
Ejector button upward to eject the used test strip. The device
will automatically turn o after the test strip is removed.
To remove the used lancet, remove the lancet from the
lancing device after you have nished testing. Discard
your used strip and lancet properly in a puncture-resistant
container.
Important!
The used lancet and test strip may be biohazards. Please
consult your health-care provider for proper disposal which
complies with your local regulations.
Control Solution Testing
Our Control Solution contains a known amount of glucose
that reacts with test strips and is used to ensure your device
and test strips are working together correctly.
Test strips, control solutions, or sterile lancets may not
be included in the kit (please check the contents on your
product box). They can be purchased separately.
Do a control solution test when:
9 you suspect the device or test strips are not working
properly.
9 your blood glucose test results are not consistent with
how you feel, or if you think the results are not accurate.
9 you have dropped or think you may have damaged the
device.
To perform the control solution test, do the following:
1.Insert the test strip into the test slot of the device. Wait for
the device to display the test strip“ “ and blood drop
“ “.
2.Press MAIN to mark this test as a control solution test. With
“QC”displayed, the device will store your test result in the
memory under “QC”. If you press MAIN again, the “QC” will
disappear and this test is no longer a control solution test.
Important!
When doing the control solution test, you have to mark
it so that the test result will NOT mix with the blood
glucose TEST RESULTS stored in the memory. Failure to
do so will mix up the blood glucose test results with the
control solution test results in the memory.
3.Apply the control solution. Shake the control solution vial
thoroughly before use. Squeeze out a drop and wipe it o,
then squeeze another drop and place it on the tip of the
vial cap. Hold the device to move the absorbent hole of the

EN-10
test strip to touch the drop. Once the conrmation window
is lled completely, the device will begin counting down.
Note:
To avoid contaminating the control solution, do not directly
apply the control solution onto a strip.
4.Read and compare the result. After counting down to 0, the
test result of the control solution will appear on the display.
Compare this result with the range printed on the test
strip vial or individual foil pack and it should fall within this
range. If the test result is out of range, read the instructions
again and repeat the control solution test.
Note:
• Do NOT test your blood.
• The control solution range printed on the test strip vial or
individual foil pack is for control solution use only. It is not a
recommended range for your blood glucose level.
• Refer to the Maintenance section for important
information about your control solutions.
Out-of-range results:
If you continue to get results that fall outside the range
printed on the test strip vial, it means that the meter and
strips might not be working properly. Please contact your
local customer service or place of purchase for assistance.
Reviewing Test Results
Your device stores the 450 most recent test results along with
respective dates and times in its memory. To enter the device
memory, start with the device switched o.
To review all test results, do the following:
1.Press and release MAIN. The“ ”icon appears on the
screen.
2.Press MAIN to review the test results stored in the device.
Press MAIN repeatedly to review other test results stored in
the device. After the last test result, press MAIN again and
the device will be turned o.
(118 mg/dL = 6.5 mmol/L;
118-160 mg/dL = 6.5-8.8 mmol/L)
118~160

EN-11
To review the day-average test results, do the following:
1.Press and hold MAIN for 3 seconds until the“ ”icon
appears. Release MAIN and then your 7-day average result
measured in general mode will appear on the display.
2.Press MAIN to review 14, 21, 28, 60 and 90-day average
results stored in each measuring mode in the order of Gen,
AC, then PC.
(100 mg/dL = 5.5 mmol/L; 200 mg/dL = 11.1 mmol/L)
(100 mg/dL = 5.5 mmol/L)
Note:
• Press and hold MAIN for 5 seconds to exit the memory
mode or leave it without any action for 3 minutes. The
device will turn o automatically.
• If using the device for the rst time, the“---”icon will appear
when you recall the test results or review the average result.
This indicates that there is no test result in the memory.
• Control solution results are NOT included in the day
average.
Announcement of Memory Result by
Universal Tone
Only the most recent result that was saved can be
announced acoustically. If you press MAIN to turn the meter
on, you will rst hear the Long-Beep which stands for power-
on and then the most recent result.
Only the average for the last 7 days is announced
acoustically. If the 7-day average cannot be calculated, three
horizontal bars are displayed. This is signaled acoustically
with 3 long beeps representing 3 zeroes.
Transferring Data
Data Transmission Via USB Cable
1.Install the software on your computer
Download Health Care System Software and instruction
manual provided on the ForaCare Suisse AG Web site:
http://www.foracare.ch. Follow the instructions to install the
software on your computer.
2.Connect the device with your computer using a USB Cable
Connect the USB cable to a USB port on your computer.
With the FORA Diamond PRIMA switched o, connect
the other end of the USB cable to the FORA Diamond
PRIMA data port. “ ”will appear on the meter display,
indicating that the meter is in communication mode.

EN-12
To change the battery, do the following:
1. Press the edge of the battery cover and lift it up to remove
the cover.
2.Remove the old battery and replace with one 1.5V AAA size
alkaline battery.
3.Close the battery cover. If the battery is inserted correctly,
you will hear a“beep”afterwards.
CAUTION RISK OF EXPLOSION IF BATTERY IS
REPLACED BY AN INCORRECT TYPE.
DISPOSE OF USED BATTERIES ACCORDING TO THE
INSTRUCTIONS.
Note:
• Replacing the battery does not aect the test results stored
in memory.
• Keep away the battery from small children. If swallowed,
promptly seek medical assistance.
• Battery may leak chemicals if unused for a long time.
Remove the battery if you are not going to use the device
for an extended period.
• Properly dispose of the used battery according to your
local environmental regulations.
3.Transfer data to your computer
Follow the software on-screen instructions to transmit data.
The data transmitted will include results with date and
time. Remove the cable and the device will automatically
turn o.
Note:
• While the meter is in transmission mode, it will be unable
to perform a blood glucose test.
Maintenance
Changing Battery
You must change the battery immediately and reset the date
and time when the battery power is extremely low and“
& ” appears on the screen. The meter cannot be turned
on.

EN-13
Caring for Your Device
• To clean the exterior of the device, wipe it with a cloth
moistened with tap water or a mild cleaning agent, then
dry the device with a soft dry cloth. Do NOT rinse with
water.
• Do NOT use organic solvents to clean the device.
Device Storage
• Storage condition: -20°C to 60°C (-4°F to 140°F), below 95%
relative humidity.
• Always store or transport the device in its original storage
case.
• Avoid dropping and heavy impact.
• Avoid direct sunlight and high humidity.
Meter Disposal
The used meter should be treated as contaminated and may
carry a risk of infection during measurement. The batteries in
this used meter should be removed and the meter should be
disposed in accordance with local regulations.
The meter falls outside the scope of the European Directive
2012/19/EU-Directive on waste electrical and electronic
equipment (WEEE).
Caring for Your Test Strips
• Storage condition: 2°C to 32°C (35.6°F to 89.6°F) for glucose
test strip, below 85% relative humidity. Do NOT freeze.
• Store your test strips in their original vial only. Do not
transfer to another container.
• Store test strip packages in a cool and dry place. Keep away
from direct sunlight and heat.
• After removing a test strip from the vial, immediately close
the vial cap tightly.
• Touch the test strip with clean and dry hands.
• Use each test strip immediately after removing it from the
vial.
• Write the opening date on the strip vial label when you rst
open it. Discard remaining test strips after 6 months.
• Do not use test strips beyond the expiry date. This may
cause inaccurate results.
• Do not bend, cut, or alter a test strip in any way.
• Keep the strip vial away from children since the cap and the
test strip may be a choking hazard. If swallowed, promptly
see a doctor for assistance.
For further information, please refer to the test strip package
insert.
Important Control Solution Information
• Use only our control solutions with your device.
• Do not use the control solution beyond the expiry date or
3 months after rst opening. Write the opening date on the
control solution vial and discard the remaining solution
after 3 months.
• It is recommended that the control solution test be done
at room temperature 20°C to 25°C (68°F to 77°F). Make
sure your control solution, device, and test strips are at this

EN-14
Symbol Information
Symbol Referent Symbol Referent
For in vitro diagnostic
use Do not reuse
Consult instructions
for use
temperature
limitation
Use by
0123
CE Mark
Batch code Manufacturer
Serial number
Dispose of the
packaging properly
after use
Keep away from
sunlight Caution
Keep Dry Sterilized using
irradiation
Use within 6 months
after opening
Do not use if package
is damaged
Disposal of waste
equipment humidity limitation
1.5V 1.5 Volts DC
Battery
Model No. Quantity
Authorised
representative in the
European Union
Medical device
Reference Values
The device provides you with plasma equivalent blood
glucose results.
Time of day Normal plasma glucose range for
people without diabetes (mg/dL)
Fasting and before
meals
< 100 mg/dL (5.6 mmol/L)
2 hours after meals < 140 mg/dL (7.8 mmol/L)
Source: American Diabetes Association (2012). Clinical Practice
Recommendations. Diabetes Care, 35 (Supplement 1): S1-100.
Please consult your doctor to determine a target range
that works best for you.
6M
SN
specied temperature range before testing.
• Shake the vial before use, discard the rst drop of control
solution, and wipe o the dispenser tip to ensure a pure
sample and an accurate result.
• Store the control solution tightly closed at temperatures
between 2°C to 30°C (35.6°F to 86°F). Do NOT freeze.

EN-15
Troubleshooting
If you follow the recommended steps but the problem
persists, or error messages other than the ones below appear,
please call your local customer service.
Do not attempt to repair the device yourself and never try to
disassemble the device under any circumstances.
Result Readings (for glucose test)
Message What it Means
< 20 mg/dL (1.1 mmol/L)
20-69 mg/dL (1.1-3.8 mmol/L)
70-129 mg/dL
(3.9-7.2 mmol/L)
70-179 mg/dL
(3.9-9.9 mmol/L)
70-119 mg/dL
(3.9-6.6 mmol/L)
130-239 mg/dL
(7.2-13.3 mmol/L)
180-239 mg/
dL (9.9-13.3
mmol/L)
120-239 mg/dL
(6.7-13.3 mmol/L)
≥ 240 mg/dL (13.3 mmol/L)
> 600 mg/dL (33.3 mmol/L)
Error Message
Error
Message
Cause What To Do
The batteries cannot
provide enough
power for a test.
Replace the battery
immediately and reset date
and time on the meter
setting.
Strip has been used. Repeat the test with a new
strip.
The blood sample
has been applied to
the strip before the
meter was ready for
the measurement.
Repeat the test with a
new strip. Apply the blood
sample when the meter
indicates that it is ready
for the measurement by
displaying a“ ”and a
“”which starts blinking.
Meter calibration
data error.
Review the instructions and
repeat the test with a new
strip. If problem persists,
contact the local customer
service for assistance.
The component of
the device might be
broken.
Meter malfunction
due to damaged
components.

EN-16
You may have
removed the strip
after applying blood,
or insucient blood
volume.
Review the instructions
and repeat the test with a
new test strip. Please make
sure you use the correct
technique and dose with
enough blood.
Ambient
temperature is
below the system’s
operation range.
System operational range
is 10°C to 40°C (50°F to
104°F). Repeat the test after
the device and test strip
have reached the above
temperature.
Ambient
temperature is
above the system’s
operation range.
Announcement of Error Message by
Universal Tone
• Hi or Lo Result:
•Results larger than 600 mg/dL (33.3 mmol/L) are
represented as 999, i.e. three groups of nine short beeps
with pauses between the groups.
•Results lower than 20 mg/dL (1.1 mmol/L) are represented
as 000, i.e. three long beeps.
• Low Battery Warning: When the batteries are about to be
exhausted, 2 quick beeps are announced three times in
succession. This warning is sounded when the meter is
switched on.
• Other Errors: Other Error Messages are announced by 2
quick beeps four times in succession.
Blood Glucose Measurement
Symptom Cause What To Do
The device
does not
display a
message after
inserting a
test strip.
Batteries
exhausted.
Replace the battery
immediately and reset
date and time on the
meter setting.
Test strip inserted
upside down or
incompletely.
Insert the test strip with
contact bars end rst and
facing up.
Defective device or
test strips.
Please contact customer
service.
The test does
not start after
applying the
sample.
Insucient blood
sample.
Repeat the test using a
new test strip with larger
volume of blood sample.
Defective test strip.
Repeat the test with a new
test strip.
Sample applied
after the device
is automatically
turned o.
Repeat the test with a new
test strip. Apply sample
only when ashing“ “
appears on the display.
Defective device. Please contact customer
service.

EN-17
The control
solution
testing result
is out of
range.
Error in performing
the test.
Read instructions
thoroughly and repeat the
test again.
Control solution
vial was poorly
shaken.
Shake the control solution
vigorously and repeat the
test again.
Expired or
contaminated
control solution.
Check the expiration date
of the control solution.
Control solution
that is too warm or
too cold.
Control solution, device,
and test strips should
be at room temperature
(20°C to 25°C / 68°F to
77°F) before testing.
Defective test strip. Repeat the test with a new
test strip.
Device
malfunction.
Please contact customer
service.
Specications
Memory 450 measurement results with respective
date and time
Dimensions 86 (L) x 53.6 (W) x 19.5 (H) mm
Power Source One 1.5V AAA alkaline battery
Weight 52.4 g (without battery)
External output USB Cable
Features
Auto electrode insertion detection
Auto sample loading detection
Auto reaction time count-down
Auto switch-o after 3 minutes without
action
Temperature warning
Operating Condition 10°C to 40°C (50°F to 104°F), below 85%
R.H. (non-condensing)
Storage/
Transportation
Condition
-20°C to 60°C (-4°F to 140°F), below
95% R.H
Measurement Units either mg/dL or mmol/L for glucose test
Measurement Range 20 to 600 mg/dL (1.1 to 33.3 mmol/L) for
glucose test
Hematocrit range 20~60% for glucose testing
Test Sample Capillary whole blood
Test Result Glucose measurements are reported as
plasma equivalents
This device has been tested to meet the electrical and safety
requirements of: IEC/EN 61010-1, IEC/EN 61010-2-101, EN
61326-1, IEC/EN 61326-2-6.

EN-18
WARRANTY TERMS AND
CONDITIONS
With respect to disposable products, ForaCare Suisse
warrants to the original purchaser that, at time of delivery,
each standard product manufactured by ForaCare Suisse
shall be free from defects in material and workmanship and,
when used for the purposes and indications described on the
labeling, is t for the purposes and indications described on
the labeling. All warranties for a product shall expire as of the
product expiration date, or if none, after two (2) year from the
original date of purchase, as long as it has not been modied,
altered, or misused. ForaCare Suisse warranty hereunder shall
not apply if:
(i) a product is not used in accordance with its instructions
or if it is used for a purpose not indicated on the labeling; (ii)
any repairs, alterations or other work has been performed by
the buyer or others on such item, other than work performed
with ForaCare Suisse’s authorisation and according to its
approved procedures; or (iii) the alleged defect is a result
of abuse, misuse, improper maintenance, accident or the
negligence of any party other than ForaCare Suisse. The
warranty set forth herein is conditioned upon proper storage,
installation, use and maintenance in accordance with
applicable written recommendations from ForaCare Suisse.
The warranty furnished hereunder does not extend to
damaged items purchased hereunder resulting in whole or
in part from the use of components, accessories, parts or
supplies not furnished by ForaCare Suisse.