FOR-A 6 Connect User manual

Multi-functional Monitoring System
Multifunktionales Messsystem
Système de surveillance multifonctionnel
Sistema de supervisión multifuncional
Owner’s Manual
Bedienungsanleitung
Manuel de I’utilisateur
Manual del propietario

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 and the blood glucose/ hematocrit/
hemoglobin test strips can be used for the testing of
newborns.
• The β-Ketone, total cholesterol and uric acid test strips shall
NOT be used for the testing of newborns.
• Before using this device, 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.
• 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 test 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 perform a test. Using
other substances will lead to incorrect results.
• If you are experiencing symptoms that are inconsistent
with your test results and you have followed all the
instructions given in this owner’s manual, contact your
healthcare professional.

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 the blood
glucose, hematocrit, hemoglobin, β-ketone, total cholesterol
and uric acid levels in whole blood. It should not be used for
the diagnosis of diabetes.
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
With dierent types of test strips, your FORA 6 Connect
Multi-functional Monitoring System allows you to measure
the amount of blood glucose, hematocrit, hemoglobin,
β-Ketone, total cholesterol and uric acid levels in whole
blood. The testing is based on the measurement of electrical
current generated by the reaction of dierent substance with
the reagent of the strip. The meter measures the current,
calculates the blood glucose, hematocrit, hemoglobin,
β-Ketone, total cholesterol or uric acid, and displays the
result.
• We do not recommend using this product on severely
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
For example:
1)120 mg/dL ÷ 18 = 6.6 mmol/L
2)7.2 mmol/L x 18 = 129 mg/dL approximately

EN-3
The strength of the current produced by the reaction
depends on the amount of the substance in the blood
sample.
Product Overview
9.Bluetooth
Indicator
4.Battery
Compartment
5. Display Screen
6. Down Button 7. MAIN Button
8. UP Button
1. Test Strip Slot
3. Test Strip Ejector
2. Strip Indication Light
Screen Display
1234
5
6
7
8
9
10
11
12
13
14
15 16
17
18
1. Blood Drop Symbol
2. Test Strip Symbol
3. Universal Tone Symbol
4. Low battery Symbol
5. Ketone Symbol / Ketone
Warning
6. Total Cholesterol Symbol
7. Blood Glucose Symbol
8. Uric Acid Symbol
9. Test Result
10. QC Mode
QC – control solution testing
11. Measurement Mode
AC - before meal
PC - after meal
Gen - any time of day
12. Memory Symbol
13. Day Average
14. Warning Symbol
15. Hemoglobin Symbol
16. Date & Time
17. Hematocrit Level
18. Measurement Unit

EN-4
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
1. The meter turns on automatically once a new battery is
inserted.
Note:
When you turn on the meter by pressing MAIN button for
the rst time, the meter will turn o automatically due to no
data.
2. Start with the meter o (no test strip inserted). Press and
hold and at the same time.
Step 2: Conguring the Settings (Date, Time, Universal
Tone, Memory Deletion and Reminder Alarm) Set [Reminder
Alarm]
Set [Minute]
Set [Year] Set [Month] Set [Day] Set [Hour]
Set [Beep On,
Universal Tone,
Beep O]
Delete Memory
Records
Set [Alarm Time
(Hour)]
Set [Alarm Time
(Minute)]
Press or to adjust the value or enable/disable the
setting. Then press MAIN button to conrm the setting and
switch to another eld.

EN-5
Note:
• Press to select Beep On, Universal Tone On or Beep O.
Press MAIN button to conrm.
• 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 the alarm, press or to change On to OFF.
Press MAIN button to conrm.
• When the alarm goes o, the device will automatically turn
on. Press to mute the alarm. If you do not press , the
device will beep for 2 minutes then switch o.
• If the device is idle for 3 minutes during the setting mode,
it will turn o automatically.
Before Testing
Calibration
You must calibrate the meter every time you begin to use a
new vial of β-ketone/ Total cholesterol/ Uric acid test strips
by setting the meter with the correct code. Test results may
be inaccurate if the code number displayed on the monitor
does not match the number printed on the strip label or strip
foil pack.
How to Code Your Meter (for β-ketone/ Total
cholesterol/ Uric acid test)
1. Insert the code strip when the monitor is o. Wait until the
code number appears on the display.
Note:
Make sure the code numbers on display, code strip, and test
strip vial or foil pack are the same. The code strip should be
within the expiry date; otherwise, an error message may
appear.
2. Remove the code strip, the display will show“OFF”. This
tells you that the meter has nished coding and is ready for
β-ketone/ Total cholesterol/ Uric acid testing.
Checking the Code Number
You need to make sure that the code number displayed on
the meter matches the number on your test strip vial or foil
pack before you proceed. If it matches, you can proceed with

EN-6
your test. If the codes do not match, please stop testing and
repeat the calibration procedure. If the problem persists,
contact Customer Service for help.
NOTICE:
The codes used in this manual are examples only; your meter
may display a dierent code.
WARNING:
• It is important to make sure that the LCD displayed code is
the same as the code on your test strip vial or foil pack before
testing. Failure to do so will get inaccurate results.
• If the LCD displayed code is not the same as the code on your
test strip vial and the code number cannot be updated, please
contact Customer Service for assistance.
Testing With Blood Sample
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.
12345
1. Blood Glucose
2. Blood Glucose / Hematocrit
/ Hemoglobin
3. β-Ketone
4. Total Cholesterol
5. Uric Acid

EN-7
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.
6.Pull the cocking control out until the orange bar appears
on the release button window.

EN-8
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 (For Blood
Glucose Test Strip Only)
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:

EN-9
• You think your blood sugar is low.
• You are not aware of symptoms when you become
hypoglycemic.
• 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.
1
2
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.
Performing A 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.Press to adjust the measuring mode, and press MAIN
button to conrm it.
• 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 the desired
site. Wipe o the rst appeared drop of blood with a clean
cotton swab. Gently squeeze the punctured area to obtain
another drop of blood. Be careful NOT to smear the blood
sample.

EN-10
The blood sample size of each test should be at least,
• blood glucose test: 0.5μL
• blood glucose/ hematocrit/ hemoglobin test: 0.5μL
• β-ketone test: 0.8μL
• total cholesterol test: 3.0μL
• uric acid test: 1.0μL
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.
BG BG
BG BG BG
BG
BG B
BG BG BG
BG
G BG BG BG BG BG
BG BG BG BG BG BG B
BG BG BG BG BG BG
G BG BG BG BG BG BG
BG BG BG BG BG BG B
GBG
5.Read your result.
The results of your 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)
Blood Glucose
Blood Glucose /
Hematocrit/
Hemoglobin
Uric Acid
β-Ketone Total cholesterol
Ketone warning
• When your blood glucose result is higher than 240 mg/
dL (13.3 mmol/L), the meter will display the blood glucose
reading as well as a Ketone warning ( ashing KETONE
and“ ” ).

EN-11
• The ketone warning is to notify you that you may be at risk
of elevated Ketone levels and a Ketone test is recommended.
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.
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 substance
that reacts with test strips and is used to ensure your device
and test strips are working together correctly.

EN-12
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
test strip to touch the drop. Once the conrmation window
is lled completely, the device will begin counting down.
BGBGBGBGBG
BGBGBGBGB
BGBGBGBGB
G
G BG BG
BG BG BG B
BG BG
G
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.
118~160
BG BG
BG BG BG B
BG BG BG B
BG BG BG B
BG BG
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 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.The meter will detect the dierence between control solution
and blood samples automatically. It will automatically mark
the result as a control solution test with“QC”display.

EN-13
Reviewing Test Results
Your device stores the 1000 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 button or . The“ ” icon
appears on the screen.
2.Press MAIN to review the test results stored in the device.
Press or 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.
Note:
• Control solution test results are stored in the memory.
• The control solution range printed on the test strip vial or
individual foil pack is for control solution use only. It is not
the recommended range or reference values.
• 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.
(100 mg/dL = 5.5 mmol/L; 200 mg/dL = 11.1 mmol/L)
To review the day-average test results, do the following:
1.Press and release to enter memory mode for average
results with“ ”and displayed on the screen.
Release MAIN and then your 7-day average result
measured in general mode will appear on the display.
2.Press or to review 14, 21, 28, 60 and 90-day average
results stored in each measuring mode in the order of Gen,
AC, then PC.

EN-14
from your FORA 6 Connect via Bluetooth. Follow the steps
below to transmit data from your FORA 6 Connect. Please
contact your local customer service or place of purchase for
assistance.
1.Install the software (iFORA HM) to your device
with an iOS or Android system.
2.Every time the FORA 6 Connect is turned o, the Bluetooth
will be initiated for data transmission. The Bluetooth
indicator ashes in blue.
3.Make sure your FORA 6 Connect is already paired with your
device with an iOS or Android system by following the
instructions as below.
Bluetooth Smart Meter
Search
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 Bluetooth
You can use your device with an iOS (5.0.1 or higher) or
Android system (4.3 API Level 18 or higher) to download data

EN-15
• Make sure your device with iOS or Android system has
turned on its Bluetooth before transmitting the data and
the meter is within the receiving range.
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.
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
Bluetooth Smart Meter
Add
Yes
Note:
This step is recommended when the user needs to pair this
meter to a Bluetooth receiver for the rst time, or when
the user needs to pair this meter to another new Bluetooth
receiver.
4.If your device with an iOS or Android system is within the
receiving range, the data transmission will start and the
Bluetooth signals in blue. Once it is nished, the FORA 6
Connect will automatically switch o.
5.If your device with an iOS or Android system is not within
the receiving range, the FORA 6 Connect will automatically
switch o in 2 minutes.
Note:
• While the meter is in transmission mode, it will be unable
to perform a blood glucose test.

EN-16
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.
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 conditions: 2ºC to 30ºC (35.6ºF to 86ºF) and below
85% relative humidity for all test strips (blood glucose,
blood glucose/hematocrit/hemoglobin, β-ketone, total
cholesterol, uric acid). 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.
• 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.

EN-17
• 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
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.
DETAILED INFORMATION
The meter provides you with plasma equivalent results.
Desirable ranges:
Normal plasma glu-
cose range for people
without diabetes *1
Fasting and before
meal < 100 mg/dL (5.6 mmol/L)
2 hours after meals < 140 mg/dL (7.8 mmol/L)
Total cholesterol *2< 200 mg/dL (5.17
mmol/L)
Uric Acid *3 Male 3.5 ~ 7.2 mg/dL (0.208 ~
0.428 mmol/L)
Female 2.6 ~ 6 mg/dL (0.155 ~
0.357 mmol/L)
A part of a complete blood count (CBC) - Capillary whole
blood sample
Hemoglobin *4Male 14 ~ 17 g/dL
Female 12 ~ 15 g/dL
Hematocrit *4Male 41% ~ 50%
Female 36% ~ 44%
• If the hematocrit test result is more than 70%, or
hemoglobin is more than 23.8 (g/dL), the blood glucose test
may be invalid. Please redo the test, and consult your doctor
if the result is repeatedly invalid.
• The β-Ketone test measures Beta-Hydroxybutyrate (β -OHB),
the most important of the three β-Ketone bodies in the blood.
Normally, levels of β–OHB are expected to be less than 0.6
mmol/L.

EN-18
• β-OHB levels may increase if a person fasts, exercises
vigorously or has diabetes and becomes ill. If your β-Ketone
result is 0.0 mmol/L, repeat the β-Ketone test with new
test strips. If the same message appears again or the result
does not reect how you feel, contact your healthcare
professional.
Follow your healthcare professional’s advice before you
make any changes to your diabetes medication programme.
If your β-Ketone result is between 0.6 and 1.5 mmol/L, this
may indicate development of a problem that could require
medical assistance. Follow your healthcare professional’s
instructions. If your β-Ketone result is higher than 1.5
mmol/L, contact your healthcare professional promptly
for advice and assistance. You may be at risk of developing
diabetic ketoacidosis (DKA).
Please consult your doctor to determine a target range
that works best for you.
*1. American Diabetes Association (2014). Clinical Practice
Recommendations. Diabetes Care, 37 (Supplement 1): S16.
*2. Third Report of the National Cholesterol Education
Program (NCEP) Expert Panel on Detection, Evaluation,
and Treatment of High Blood Cholesterol in Adults (Adult
Treatment Panel III) nal report(2002).Circulation106:
3143–3421
*3. National Kidney Foundation (2014)
*4. NIH - National Heart, Lung, and Blood Institute (NHLBI)
https://www.nhlbi.nih.gov/health-topics/blood-tests
Symbol Information
Symbol Referent Symbol Referent
For in vitro diagnostic
use Do not reuse
Consult instructions
for use
Storage/Transportation
temperature limitation
Use by CE Mark
Batch code Manufacturer
Serial number
Dispose of the
packaging properly
after use
Keep away from
sunlight
Caution, consult
accompanying
documents
Keep Dry Sterilized using
irradiation
Model number Do not use if package is
damaged
Disposal of waste
equipment Storage/Transportation
humidity limitation
1.5V 1.5 Volts DC
Quantity Battery
Authorised
representative in the
European Union
Unique device
identier