Microlife GlucoTeq Handleiding

Microlife Bloedglucosemeter GlucoTeq

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GlucoTeq - BGM 200

IB BGM 200_mg EN 5120 - Revision Date: 2020-12-11

Explanation of Symbols

For In vitro diagnostic use Temperature limitation

Please consult instructions for use Use by / Expiry date

Do not reuse Manufacturer

Lot number Caution, consult accompanying document

Keep dry Keep away from sunlight

Humidity limitation EU representative

This product fulfils the requirements of Directive 98/79/EC in vitro diagnostic medical

device.

Do not use if package is damaged Serial number

Wholecare

Biomedical Corporation

8F, 443, RuiGang Road, NeiHu

Taipei, 11492, Taiwan

Medical Device Safety Service GmbH

(MDSS GmbH)

Schiffgraben 41

30175 Hannover / Germany

LOT

0123

Overview

1.Before you begin

2.Getting to know your system

3.Prepare for blood sampling

4.Performing blood test

5.Alternative site testing

6.Control solution testing

7.Memory recall

8.Caring for your meter and test strip

9.Specifications

10.System Troubleshooting

11.Performance Characteristics

12.Guarantee

1. Before you begin

Please read this before using.

The following basic safety precautions should always be taken.

1.Close supervision is necessary when the device is used by, on, or near children or people with disabil-

ities.

2.Use the device only for the intended use described in this user guide.

3.Do not use test strips and control solutions which are not supplied by the manufacturer.

4.Do not use the device if it is not working properly, or if it has suffered any damage.

5.Before using any product to test your blood glucose, read all instructions thoroughly and practice the

test. Do all quality control checks as directed and consult with a diabetes healthcare professional.

Keep this user guide with you.

Intended use:

Principle of Measurement

Blood glucose is measured by an electrical current that is produced when a blood sample mixes with

the reagent (special chemicals) of the test strip. The electrical current changes with the amount of

glucose in the blood sample. The Microlife GlucoTeq meter measures the strength of the electrical

current, calculates your blood glucose level and then displays your result in either milligrams of glucose

per deciliter (mg/dL) or millimoles of glucose per liter (mmol/L).

Caution

1.The user should not take any decision of medical relevance without first consulting his or her medical

practitioner.

2.Call your doctor immediately if you experience symptoms that are not consistent with your blood

glucose test results.

3.High altitudes above 3,402 meter (11,161 ft) may affect the test results.

4.Temperatures outside the range of 10°C to 40°C (50°F to 104°F) may affect the test results. Do not

test outside of these temperature ranges.

5.Do not perform servicing and maintenance while the meter is in use.

6.Modification of this equipment is not allowed. If the equipment is used in a manner not specified by

the manufacturer, the protection provided by the equipment may be impaired.

7.Do not use this meter near cellular or cordless telephones in a call, walkie-talkies, garage door

openers, radio transmitters, or other electrical or electronic equipment that are sources of electromag-

netic radiation, as these may interfere with the proper operation of the meter.

Important Health-Related Information

1.Apply only capillary whole blood sample to test your blood glucose. Applying other substances or

plasma, serum will cause wrong results.

2.Severe dehydration and excessive water loss may cause false low results. If you believe you are

suffering from severe dehydration, consul essional immediately.t your healthcare prof

3.Test results below 60 mg/dL (3.3 mmol/L)*1 indicates low blood glucose (hypoglycemia). Test results

greater than 240 mg/dL (13.3 mmol/L)*2 indicates high blood glucose (hyperglycemia).If your results

are below 60 mg/dL (3.3 mmol/L) or above 240 mg/dL (13.3 mmol/L), repeat the test, and if the results

are still below 60 mg/dL (3.3 mmol/L) or above 240 mg/dL (13.3 mmol/L), consult your healthcare

professional immediately.

4.Inaccurate results may occur in severely hypotensive individuals or patients in shock. Inaccurate low

results may occur for individuals experiencing a hyperglycemic-hyperosmolar state, with or without

ketosis. Critically ill patients should not be tested with blood glucose meters.

5.Abnormal red blood cell counts may cause false results. Please consult your healthcare professional

if you do not know your hematocrit level.

6.Interference: Reducing substances occurring in the blood naturally (uric acid, bilirubin) or from thera-

peutic treatments (ascorbic acid, acetaminophen) will not significantly affect Microlife GlucoTeq test

results. However, elevated concentrations of these substances may affect test results. The

compounds listed in the table were found to have no affect at the concentration indicated.

REFERENCE:

Kahn, R. and Weir, G.: Joslinis Diabetes Mellitus, 13thed Philadelphia: Lea and Febiger (1994), 489. *1

Krall, L.P. and Beaser, R. S.: Joslin Diabetes Manual. Philadelphia: Lea and Febiger (1989), 261-263. *2

2. Getting to know your System

The Microlife GlucoTeq Glucose Monitoring System

The Microlife GlucoTeq system uses the latest technology to provide you with easy and comfortable

testing. The system requires only 0.5uL blood sample to complete the testing in only 5 seconds.

Please review the contents of your purchase to confirm that all the components are included as listed

on the side of your meter box.

The system is intended for use outside the body (in vitro diagnostic use only). It should be used

only for self-testing blood glucose (blood sugar) and only with fresh capillary whole blood

samples. The system is intended for use in the home and in clinical settings. The system should

not be used for the diagnosis of diabetes or for the testing of newborns.

Compounds Concentrations higher than the following values may cause

inaccurate results

Acetaminophen 8.0 mg/dL (0.53 mmol/L)

Ascorbic Acid 5.0 mg/dL (0.28 mmol/L)

Aspirin 60 mg/dL (3.33 mmol/L)

Bilirubin 90 mg/dL (1.54 mmol/L)

Cholesterol 500 mg/dL (12.9 mmol/L)

Creatinine 5.0 mg/dL (0.44 mmol/L)

Dopamine 2.0 mg/dL (0.11 mmol/L)

EDTA 360 mg/dL (12.3 mmol/L)

Galactose 900 mg/dL (50 mmol/L)

Gentisic Acid 5.0 mg/dL (0.32 mmol/L)

Glutathione 53 mg/dL (1.72 mmol/L)

Haemoglobin 500 mg/dL (0.08 mmol/L)

Heparin 8,000 U/dL

Hydroxyurea 3.0 mg/dL (0.39 mmol/L)

Ibuprofen 50 mg/dL (2.42 mmol/L)

Icodextrin 13 mg/dL (0.01 mmol/L)

L-dopa 10 mg/dL (0.51 mmol/L)

Maltose 900 mg/dL (26.3 mmol/L)

Methyldopa 3.0 mg/dL (0.13 mmol/L)

Pralidoxime Iodide 25 mg/dL (0.94 mmol/L)

Salicylate 60 mg/dL (4.34 mmol/L)

Tolazamide 100 mg/dL (3.21 mmol/L)

Tolbutamide 400 mg/dL (14.8 mmol/L)

Triglycerides 2,000 mg/dL (22.6 mmol/L)

Uric Acid 8.0 mg/dL (0.48 mmol/L)

Xylose 100 mg/dL (6.66 mmol/L)

1Illuminated Test Strip Slot

Insert the test strip here. The meter will turn on auto-

matically and the slot LED light will illuminate.

To track the position of test strip slot without strip

inserting, press main button

and the slot LED light will be flashing.

2LCD Display

Guides you through the test using symbols and

simple messages.

3Main Button

Turns the meter on or performs other functions

described in this user guide.

4Data Port

Allows you to transfer the information stored in the

meter to a computer to view, analyze and print.

5Set Button

Located on the back of the meter, inside the battery

compartment; used to set up the meter.

6Battery Compartment

Holds ONE 3V Lithium battery (battery type

CR2032). Please install battery into meter before

you start testing.

7Meter Label

Each meter has its unique number on it. Do not alter

or tear the label off.

vcc

GND

If any part of the display is not working, contact your local distributor for help.

Battery

Microlife GlucoTeq meters come with one (1) CR2032 lithium battery. The battery is manufactured in a

charged state and not designed for recharging. Recharging the battery can cause battery leakage, or

in some cases, high pressure rupture.

Warning: Batteries can explode or leak and cause burns if installed backwards, disassembled,

charged or exposed to water, fire or high temperatures.

Low Battery

The meter will alert you when the power is getting low by displaying two different messages:

When the battery symbol AR appears alone on the display, the meter is functional and the results

remain accurate, but you should change the battery as soon as possible.

When the battery symbol AR appears together with the «E-b» symbol on the display, the battery does

not have enough power for a test. You must change the battery before using the meter.

Replacing the battery does not affect the meter’s memory (previous test results stored in

memory). However, the date, time and unit settings may need to be updated; update the settings

by following the steps in «Setting Time and Date».

As with all small objects, the battery should be kept away from small children. If the battery is swal-

lowed, seek medical assistance immediately.

Remove the battery if you are not going to use the device for a long period of time (i.e. 3 months

or more), or the battery might leak chemicals.

Please discard the product or the batteries properly according to the regulations of your country.

Setting Mode

Please install battery first and complete the setting before you begin to test.

8Contact Bars

Insert this end of the test strip into the meter. Push

it in firmly until it will not go any further.

9Test Strip Handle

Hold this part to insert the test strip into the test strip

slot on the meter.

AT Confirmation Window

Shows whether enough blood has been drawn into

the test strip’s absorbent channel.

AK Absorbent Channel

Apply a drop of blood and it will be drawn in auto-

matically.

AL Test Result Area

Displays test results.

AS Unit of Measure

Indicates what unit of measure

the test result is displayed in.

AM Appears when test result is

lower than 70 mg/dL (3.9

mmol/L) or higher than 180

mg/dL (10 mmol/L).

BT Temperature Symbol

Appears when temperature is

outside of operating range.

Appears when test result is

within the range of 70 to 120

mg/dL (3.9 mmol/L to 6.7

mmol/L).

BK Control Solution Test

Symbol

Shows that you are in control

solution mode.

AN Ketone Symbol

Appears when test result is

higher than 240 mg/dL (13.32

mmol/L).

BL Memory Symbol

Appears when you review the

memory.

AO Alarm Symbol

Appears when you are

setting alarms.

BM After Meal

Indicates that your test is an

After Meal test.

AP Test Strip Symbol

Appears when the meter is in

testing mode.

BN Before Meal

Indicates that your test is a

Before Meal test.

AQ Blood Drop Symbol

Flashes when sample should

be applied.

BO Date

AR Low Battery Symbol

Appears when the battery

power is low.

BP Time

STEP 1: With the meter off, press

the mark on the battery cover

and slide up to open the cover.

STEP 3: Replace with a new

battery. Be sure to align the

battery properly with the positive

(+) side up.

STEP 2: Remove the old battery

by pressing on the buckle beside

the battery and gently pulling it at

the same time.

STEP 4: Close the battery cover.

If the meter does not power on

and enter setting mode after you

have replaced the battery, check

that the battery is correctly

installed.

STEP 1: Enter Setting Mode

If your meter is off, press the SET

button 5 located in the battery

compartment. The meter is now

in the setting mode.

STEP 4: Set the Date

Press and release the main button

to advance the date. With the

correct date on the display, press

the

SET

button

and the time

will appear on the display with the

hour segment flashing.

STEP 2: Set the Year

Press and release the main button

to advance the year. With the

correct year on the display, press

the

SET

button

and the date

will appear on the display with the

month segment flashing.

STEP 5: Set the Hour

Press and release the main

button 3 to advance the hour.

With the correct hour on the

display, press the SET button 5

and the minutes segment will

start flashing.

STEP 3: Set the Month

Press and release the main button

to advance the month. With the

correct month on the display,

press the

SET

button

and the

date segment will start flashing.

STEP 6: Set the Minutes

Press and release the main

button

to advance the minutes.

With the correct minutes on the

display, press the

SET

button

and the

«OFF»

will start flashing.

Fig. A STEP 7: Set the Alarm

The meter allows you to set 4 different alarms with an order from 1 to 4.

will be displayed during the alarm setting.

Fig. B 1 - Press the main button3 to turn the alarm ON (Fig.A) or OFF (Fig.B).

2 - Press SET button 5 to move to hour setting for alarm. (Fig.C) Use the

main button 3 to set your desired hour.

Press SET button5 again to set the minute. (Fig.D).

Fig. C 3 - Press SET button to set the next alarm.

4 - Repeat step 1-3 to set the second, third and fourth alarm.

After completing fourth alarm, the AC/PC will start flashing.

Fig. D

STEP 8: Set AC/PC

Press and release the main button to select ON/OFF. With the correct 3

setting, press the SET button 5 for confirmation.

STEP 9: Delete Memory

If you do not want to clear the memory, press the SET button again to skip

this step.

If you want to clear ALL memory, press the main button for five (5) seconds.

The «- - -» will appear to indicate all memory has been deleted and the meter

will turn off.

STEP 10: Complete Setting

Setup is now complete. «OFF» is displayed and the meter will turn off.

9 AT

AO AP AQ

BP BO

vcc

GND

vcc

GND

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GND

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GND

3. Prepare for blood sampling

If your lancing device did not come with a lancing device insert, the following information shall take

the place of the insert.

Microlife LD-100 Lancing Device

Your lancing device and lancets are used for obtaining blood samples from the puncture site.

Special Features

Intended Use: The lancing device is intended for use by a single person with the lancet puncturing

through the skin for collecting blood sample.

Safety Switch design: when the depth adjustable cap is open, the trigger will be relieved automatically

which prevents users from being pricked if you are not intended to start the test. You can eject the used

disposable lancet on one hand operation by pushing the plunger with your thumb at this status.

When the cap is closed, it will lock the lancet eject function and prevent the lancet from being removed

when you are intended to start the test.

Stable and sophisticated structure design ensures almost no vibration, so that the lancet pricking is

steadier with almost no pain. It lowers the psychological pressure of users very much and let people

recover the test frequencies which recommended by HCPs.

A stylish, slim and ergonomic design is very convenient and user friendly.

Clear indication for depth penetration (numeric display): easy to read and adjust for users.

Important Lancing Device and Lancets Information

1.Lancet is for single use only.

2.Keep lancing device and lancets clean.

3.Use caution when removing the used lancet from the device and when disposing the used lancet.

The meter and lancing device are for single patient use.

Do NOT share them with anyone including family members.

Do NOT use on multiple patients.

Setting your Lancing Device

4. Performing a Blood Test

1A stylish, slim and ergonomic design is very

convenient and user friendly.

2Big window to show the penetration depth with

numeric display which is easy for the user to

read.

3Big release button, comfortable and easy to

operate.

4Patented feature of lancet ejection by one

thumb pushing with only one hand operation.

5Patented safety switch design:

when the cap is closed, it allows only load but

lock the function of lancet ejection. When cap

is open, it allows lancet ejection but release the

trigger automatically to prevent accidental

pricking.

6Depth adjustable cap

7Release button

8Plunger

9Hub

AT Clear cap (optional)

AK Disposable lancet (optional)

1. Hold the depth adjustable

cap in one hand and hold

hub in the other hand, twist

off the depth adjustable

cap.

5. Select a depth of pene-

tration by rotating the top

portion of the depth adjust-

able cap until the number

matched to the window.

Settings are based on skin

type.«1,2» are for

soft or thin skin. «3,4» are

for average skin.

«5,6» are for thick or

calloused skin.

2. Insert a new disposable

lancet firmly into the lancet

holder.

6. Hold the hub in one hand

and push on the plunger in

the other hand. The device

will be cocked.

Release the plunger; it will

go back to its original posi-

tion near the hub.

3. Twist off and set aside

the protective cover of the

disposable lancet.

4. Replace the depth

adjustable cap.

The Lancing device is made by

MEDIFUN CORPORATION

No.8, Shuyi Rd., South Dist., Taichung

City, 40241, Taiwan (R.O.C.)

1. Wash Your Hands and the Puncture Site:

Wash your hands in warm, soapy water. Rinse and dry completely. Warm your

fingers to increase blood flow.

2. Insert Test Strip:

Remove a new test strip from vial. Be sure to tightly replace vial cap after

removing test strips. Insert a test strip with the contact bar end entering into the

test strip slot first. Push the test strip as far as it will go without bending it. The

meter turns on automatically.

*To track the position of test strip slot, press main button and the slot LED light will flashing.

3. Select and Lance a Puncture Site:

Hold the prepared lancing device firmly against the side of your fingertip. Press

the release button.

NOTE: If you want to do alternative site testing, please refer to the «About Alter-

native Site Testing (AST)» section. Please consult your healthcare professional

before obtaining blood from site other than your fingertip.

4. Obtain a Blood Sample:

Gently massage your finger or puncture site to obtain the required blood

volume. To perform the test, you need only 0.5 μL of blood sample. Do not

smear the blood sample. To obtain best accurate result, wipe off the first drop

of blood and gently squeeze another drop of blood.

5. Apply Blood Sample:

When the meter shows the «» symbol, apply blood to the opening of the absor-

bent channel of the test strip where it meets the narrow channel. Blood will be

drawn into the test strip. If the test strip confirmation window is full, you will hear

a beep.

6. Read Your Result:

After the meter counts down from 5 to 1, your blood glucose test result appears

along with the unit of measure, date and time.

7. Turn Off the Meter:

This blood glucose result is automatically stored in the meter memory. Turn the

meter off by removing the test strip. Discard the used test strip carefully to avoid

contamination.

8. Remove the Adjustable Comfort Tip:

After use, put the Protective Cap back onto the exposed needle of the lancet.

9. Dispose the used lancet correctly:

Slide the Lancet Ejector forward and dispose the used lancet in an approved

container. Dispose the used lancet according to your country's safety regula-

tions. Replace the Lancing Device Cap.

1 2

6 7

3 4

Incorrect Correct

GlucoTeq

Blood Glucose Monitoring System

EN Instruction Manual

Model No: BGM 200

ood

odel No: B

M 200

Product specificaties

Merk:	Microlife
Categorie:	Bloedglucosemeter
Model:	GlucoTeq

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