FOR-A 6 GTel User manual

Cellular Multi-Functional Monitoring System
Système de surveillance cellulaire multifonctionnel
Sistema de monitorización multifuncional móvil
Owner’s Manual
Manuel de I’utilisateur
Manual de instrucciones

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 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.
• 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 and storage are 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.
• 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

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, ß-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 GTel Multi-
functional Monitoring System allows you to measure the
amount of blood glucose, 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, β-Ketone,
total cholesterol or uric acid, and displays the result.
The strength of the current produced by the reaction
depends on the amount of the substance in the blood sample.
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
Product Overview
1. Test Strip Slot with Strip Indication Light
2. Power Button
3. Power Indicator
4. Home Button
5. Display Screen
6. Test Strip Ejector
7. Battery Compartment
8. Service Button
9. USB Port
Screen Display
1. Measurement Mode 6. Last Result
2. Sync 7. Date & Time
3. Logbook 8. Battery Symbol
4. Settings 9. RF Symbol
5. Two-way Message
NOTE:
• Your meter display alternates between two kinds of results
every 3 seconds, one being your last measurement result,
and the other being your blood glucose 7-day average.
• If there are no records in memory, the meter displays“---”.

EN-4
Getting Started
Initial Setup
Step 1: Enter the Setting Mode
Power on the meter (with no test strip inserted). Tap Settings
on the Main Page.
1. Setting the reminder alarm
Tap Alarm on the Settings page.
Your meter has four reminder alarms. Tap the time eld to set
the alarm time. Tap ON/OFF to enable/disable alarms.
2. Choosing a language
Tap Language on the Settings page. Select the appropriate
language for use. Tap Back.
3. Setting the speaking volume
Tap Volume on the Settings page.
There are four (4) speaking volume levels to choose from.
Select the desired speaking volume. Tap Back.
4. Setting the time
• Tap Time on the Settings page.
• Tap or to set the correct date. Press OK.
• Tap or to set the correct time. Press OK.
5. Setting the ight mode
Tap Flight mode on the Settings page to switch ON/OFF ight
mode.

EN-5
6. Setting the hi/low range for blood glucose measuring
parameters
Tap Next on the bottom of Settings page to go to the next
settings page. Tap BG Range.
Glucose:
• Three measuring modes are displayed on the screen: No
Tag/Before Meal/After Meal. Tap each mode to set the hi/
low range for each measurement.
• The hi/low range will affect the background color of your
glucose test result.
• If your test result is higher than the normal range, the
background will be red. If it is lower than the normal range,
the background will be yellow. The background will be
green when readings are within the set threshold.
Note:
• You may set it up to four reminder alarms.
• When the alarm goes o, the device will automatically turn
on. Press the HOME button or the Power button the mute
the alarm, or insert a test strip to start the measurement.
• If you do not mute the alarm, the device will beep for 2
minutes and then switch o.
• If the device is idle for 1 minute, it will enter power-saving
mode. Press the HOME button to resume.
• If the device is idle for 3 minutes, it will automatically turn
o.

EN-6
pack before you proceed. If it matches, you can proceed with
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.
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. Power on the meter and insert the code strip. 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 and the meter will return to the
home page. 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

EN-7
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.
1. Blood Glucose
2. β-Ketone
3. Total Cholesterol
4. Uric Acid
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.

EN-8
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.
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.

EN-9
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:
• 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.

EN-10
• 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. Power on the meter.
(Do NOT insert a test strip before powering on the meter)
2. Tap Measure or insert the test strip to start a measurement.
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.
The blood sample size of each test should be at least,
• blood glucose 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.
5. Read your result.
The results of your test will appear after the meter counts
down to 1. The results will be stored automatically in the
meter memory.

EN-11
6. Select your measuring mode.
• 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.
7. Data Transmission
The meter automatically transmits new data after each
measurement.
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.

EN-12
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.
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. Power on the meter.
(Do NOT insert a test strip before powering on the meter)
2. Tap Measure or insert the test strip to start a
measurement.
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 1,
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.

EN-13
100-165
Result
Glucose strip QC
120
mg/dL
12:25 pmJan-29 2017
Please remove
test strip
B
G
B
BG
BG BG
B
BG
BG BG
B
B
G BG BG
B
B
G B
G
Note:
• 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.
• For the Total Cholesterol and Uric Acid control solution
tests, tap «QC» to save the results on the «QC» tag.
• 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.
Reviewing Test Results
Your device stores the 1000 most recent test results along
with respective dates and times in its memory. To enter the
meter memory, tap the Logbook icon on the Main Page.
To review all test results, do the following:
1.Tap Logbook icon on the Main Page
The rst reading you see is the last test result along with
date, time and the measurement mode.
2.Press or repeatedly to review other test results stored
in the device.
To review the day-average test results, do the following:
1. Tap AVG tab
Your 7-, 14-, 21- day average results measured in No Tag
mode will appear on the display. Tap or to review
28-, 60-, 90- day average results.
2. Tap Before Meal/After Meal to review 7-, 14-, 21-, 28-,
60- and 90- day average results stored in each measuring
mode.
3. Exit the meter memory
Press the Home button to return to the Main Page.

EN-14
1. To initiate transmission
(a) The meter starts the transmission automatically after each
measurement, sending the new data and previous data that
has not been sent.
(b) With the meter turned on, press Sync to initiate
transmission for test results that have not been uploaded.
2. During transmission
When the arrow symbol shows up, the data transmission
has started. The message “Upload OK”will appear when the
transmission is nished.
Note:
• 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.
Transferring Data
Data Transmission via Mobile Network
The meter could upload test results to a data system through a
mobile network if your healthcare provider needs to collect the
data remotely. Usually, the settings and the SIM card deployment
should have already been placed in the meter when you receive
it. The test results will be uploaded right after every measurement
without a manual transmission. The data will be encrypted during
transmission and only the service provider can decipher it. No
personal identity will be revealed in the transmission payload.
Following the instructions of your care service provider should
enable you to get connected with the service contact. When you
use the meter for the very rst time, it’s highly recommended that
you contact your service provider to conrm that the transmission
to your account at the server side is correct and successful.
To learn more about the service procedure or transmission,
please contact the customer service of your service provider. Data
transmission is an optional function that depends on your service
provider. You may perform measurements without this function.

EN-15
3. After transmission
The uploaded results will change colors to indicate their
statuses.
Note:
• While the meter is in transmission mode, it will be unable
to perform a blood glucose test.
• Poor signal quality may be caused by busy service or no
cellular reception nearby.
• If you receive a poor signal message, take the device to a
spot with better reception and try again. Keep away from
the microwave or other devices that may interfere with
the signal.
• While the ight mode is turned on, the meter will not be
able to transmit data.
• Do not remove or replace the SIM card arbitrarily. The
data transmission might be interrupted due to improper
placement of the card. The SIM card is dedicated to
assigned servers and is not compatible with general-
purpose phone sets. Please contact your service provider
for further instructions on any transmission problems.
If Data Transmission Is Unsuccessful
If the Internet signal is unstable, your device may not be able
to communicate with your destination account at that time.
If the device cannot communicate with your account, the
following the message will appear:“Poor signal”
Your results will be stored in the logbook and the upload will
resume after the next measurement and when the signal
is stable. You can also tab Sync on the screen to restart the
upload when there is a reliable signal.
Data Security
The device will only transmit your measurement data
in a secured and encrypted way to the data server that
your service provider manages. No personally identiable
information will be covered and revealed. Please contact
your service provider to learn more about their privacy policy
regarding your measurement data.
When you use the meter for the very rst time, it’s highly
recommended that you contact your service provider to
conrm that the transmission to your account at the server
side is correct and successful.
If you wish to cancel the data transmission function, please
contact your service provider.
TWO-WAY MESSAGES
FORA 6 GTel is equipped with two-way message function
to provide you with health tips and reminders. Types
of messages include yes/no questions, multiple-choice
questions and alert messages. You can click on the answer

EN-16
icons to answer the questions.
After entering the message box, the screen displays the most
recent message. You can click Previous or Next button to
move to the previous or next message.
You can upload your answer onto the database and
download new messages from the website. Press Home
Button to return to the Main Page.
SERVICE BUTTON
The meter is equipped with a Service Button.
Pressing and holding the button for more than 3 seconds will
send a Request Assistance to the care service provider.
For more information about the Service Button, please
contact customer service or your healthcare professional.
Warning:
The Service Button is not intended for an emergency. Please
DO NOT expect an instant response or immediate assistance
by pressing this button. Your care service provider will dene
the service agreement with you.
Maintenance
Battery
Your meter comes with one 3.7V Li-ion rechargeable battery.
Low Battery Signal
The meter will display the message «Low battery» with a
«Warning Symbol» to alert you when the meter power is
getting low.
The power is not enough to do a test. Please recharge the
battery immediately.
Recharging the battery
The power adapter can be used as the battery charger when
you need to recharge the Li-ion battery. To recharge the 3.7V
Li-ion battery, connect the AC adapter to the meter and a
power source.
The power indicator will light up in red, which indicates the
battery is undergoing a recharge. It should take approximately
5 hours to be fully charged. If the power indicator is blinking
in red when connecting the AC adapter to a power source,
this indicates the meter is in a pre-charging stage. If the power
indicator starts blinking in green, this indicates the recharge
is nearly nished. The power indicator will diminish when the
recharge completes.
CAUTION:
The Li-ion battery must be recharged with the FORA 6 GTel
meter by connecting the AC adapter to an electrical outlet.
Only this 3.7V rechargeable Li-ion battery (battery model no.
ICP553136ARM) can be recharged by FORA 6 GTel with the
connection of the AC adapter. Any other kind of rechargeable
battery is not allowed or it may damage the meter.
CAUTION

EN-17
RISK OF EXPLOSION IF BATTERY IS REPLACED BY
AN INCORRECT TYPE.
DISPOSE OF USED BATTERIES ACCORDING TO THE
INSTRUCTIONS.
Note:
• FORA 6 GTel can use one Li-ion rechargeable battery ONLY
(battery model no. ICP553136ARM).
• Wrong types of batteries may cause an explosion.
• Do not use other types of batteries, mixing old and new or
batteries of dierent brands. Use only new batteries of the
specied size and type.
• Replacing the batteries does not aect the test results
stored in the memory.
• Keep the battery away from small children. If swallowed,
promptly seek medical assistance.
• Batteries might leak chemicals if unused for a long time.
Remove the batteries if you are not going to use the device
for an extended period.
• Properly dispose of the batteries 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,
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.

EN-18
• 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.
• 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)
• The β-Ketone test measures Beta-Hydroxybutyrate (ß -OHB),
the most important of the three β-Ketone bodies in the blood.
Normally, levels of ß –OHB are expected to be less than 0.6
mmol/L.
• ß -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