Goodlife AC-300 User Manual

PACKAGE BEFORE USING THIS SYSTEM. IF YOU FIND ANY IMPERFECTION IN OUR PRODUCTS, PLEASE RETURN THE WHOLE SYSTEM TO THE PLACE OF PURCHASE.
Blood Glucose Meter
Study this diagram and become familiar with all the parts of your GoodLife AutoCode AutoCode Series Blood Glucose Meter.
AC-300
STRIP SLOT: Holds a Blood Glucose Test Strip or Check Strip in place when you perform blood glucose test or perform check test.
DISPLAY: The large, easy to read display shows the test re­sults, messages, blood glucose results stored in memory, time and date.
BUTTON: Press button to enter date and time setting,or enter memory mode to recall the information stored in meter’s memory.
EJECTION BUTTON: For a easy ejection of the test strip.
Meter SN Label: The label shows the meter serial number.
BATTERY COMPARTMENT: Holds one 3V Lithium battery. Battery is not yet installed into meter when new purchas­ing. Before using the meter, please install the battery rst.
Meter LCD Window
Y
TEST RESULT
BATTERY SYMBOL: Appears when battery is low.
STRIP SYMBOL: Appears when the test strip is inserted and meter is ready for blood testing. Replace vial cap after re­moving test strips.
DATE: Month/Day at the moment of the test.
CODE: Code appears to indicate code number. when ready to test.
:Year at the moment of the test.
THERMOMETER SYMBOL: Appears when ambient temper­ature is above or below the acceptable range needed for testing.
mmol/L: Units of measure.
:Memory capacity is 900 entries. The display shows to ensure that all digits are working properly.
TIME: 12 and 24 hour period format.
: Appears to indicate memory mode when reading pre-
vious results.
SYMBOL: The test can be adjusted and stored into 2 types of test modes - BEFORE A MEAL TEST ( ), and AFTER A MEAL TEST ( ).
Blood Glucose Test Strip
Aperture: apply the blood from the front of strip
Blood Reaction Zone: It must be lled with blood entirely.
Black Electrode End: insert this end of test strip into meter.
IMPORTANT TEST STRIP INFORMATION
1. GoodLife System measures the amount of glucose in capillary whole blood. Blood can be applied to the front of the test strip and is automatically drawn to the test strip through capillary action.
2. GoodLife Blood Glucose Test Strips are intended for in vitro diagnostic use with capillary whole blood or GoodLife
Glucose Control Solution. Results will not be accurate if used with plasma or serum samples.
3. Do not use test strips beyond the expiration date indi­cated on the strip vial label.
4. The discard date for test strips is 90 days after first opening the vial. Record the discard date on the vial when you open a new vial of test strips.
5. Blood Glucose Test Strip can be damaged by heat and light. Keep the m sealed in the original v ial.
6. Store the vial in a cool, dry place below to
40°C / 104°F and above 10°C / 50°F. Do not refrigerate.
7. Do not use damaged test strips in any way. Use test strip immediately after taking it out from the vial or foil packet; replace the vial cap and close it tightly.
8. Do not transfer test strips to a new vial. Always carr y test strips in their ori ginal vial.
9. D o not place in direct heat or sunlight.
10. Do not carry loose test strips in your carrying case.
11. Test strips are for single use only.
Glucose Control Solution (Optional)
GoodLife Glucose Control Solution is used to check if the GoodLife Blood Glucose Meter and Test Strip are working correctly as a sy stem. It can be used in two ways: To practice the test procedure To make sure that the GoodLife Blood Glucose Meter and Test Strips are working together prop­erly.
IMPORTANT INFORMATION
1. Do not use control solution beyond the expiration date in­dicated on the bottle label.
2. The discard date for control solution is 90 days after rst opening. Record the discard date on the bottle when you open a new bottle of control solution.
3.
30 86
Store the control solution closed at tempera­tures between 10ºC (50ºF) and 30ºC (86ºF).
4. Please carefully read the label before use.
Perform Control Test
1. Insert a new tes t strip into the strip slot, the meter will acti­vate.
2. The code number will appear on the screen. Compare the code number shown on the screen against the code num­ber on the test strip vial. If the two numbers match, you may begin test, otherwise consult your local distributor.
3. Press button 3 times to choose Level1 control solution test (display “qCL“) or 4 times to Level2 control solution test (display “qCH“)
4. Gently shake the control solution and apply a drop to the aperture of strip. Make sure that the control solution has saturated the Blood Reaction Zone of the test str ip.
5. Test result will show up in 5 seconds. The result should correspond to the range printed on the label of strip vial used.
NOTE: REPEAT TEST IF THE RESULT FALLS OUTSIDE THE CONTROL RANGE. IF YOU CONTINUE TO GET THE RESULT FALLING OUTSIDE THE CONTROL RANGE, YOUR METER AND STRIP MAY NOT BE WORKING PROPERLY. DO NOT USE THE SYSTEM TO TEST YOUR BLOOD UNTIL YOU GET A TEST RESULT FALLS WITHIN THE CONTROL RANGE. CON­SULT YOUR LOCAL DISTRIBUTOR FOR HELP.
Check Strip
The Check Strip can be used in 2 ways:
1. To check that the meter is operating properly. Use when performing qual­ity control check on your meter.
2. To delete all test memories.
CHECK
How to check meter by check strip
1. Insert the check strip into strip slot with label side up as above.
2. You should obtain an “OK“ reading within 10 seconds, which means your meter is working properly.
3. Remove the check strip to exit. Meter will automatically turn o.
NOTE: IF YOU DO NOT GET “OK” READING BUT APPEAR OTHER ERROR MESSAGE, TURN OFF THE METER BY REMOVE CHECK STRIP FROM THE METER. THEN CHECK THE BATTERY AND REPEAT THE TEST. IF THE SECOND RES ULT PERSISTS, CONSULT YOUR LOCAL DISTRIBUTOR FOR HELP.
How to delete memory
1. Insert check strip into strip slot with label side up.
2. After “OK” displayed, press and hold the button for 3
seconds, the meter will display “dEL”, then press and hold the button for 2 seconds. Meter will display “OK” before turning o and all the memories have been de­leted successfully.
3. Remove the check strip from the meter.
Setting Meter Parameters
Setting Time & Date
When you rst time installing the batter y into the meter or when replacing a battery, the meter will automatically enter to the setting mode. Please s et correct time and date before you begin tes ting.
How to set time and date:
1. Press button to select the desired year.
2. After year is set ,allow it to ash for 3 times and shift to
the next setting.
3. Repeat above steps to set the month, day, hour and minute by Button.
4. After minute is set, the meter will display “OK” before turning o.
Prepare for Blood Sampling
Adjustable Lancing Device
Lancet
5
Protective Cap
Depth Selector
Cocking Control
Release Button
Lancet Holder
Depth Adjustment Cap
Ejection Button
IMPORTANT TEST STRIP INFORMATION
1. Lancet is for single use only.
2. Keep lancing device and lancets clean.
3. Be cautious when removing the used lancet from the device and when disposing the used lancet.
4. The lanc ing device and lancets are in conformity with MDD 93/42/EEC. Refer to product labels for contact in­formation of manufacturer and CE marking.
Set Lancing Device
1. Remove the depth adjustment cap. Insert a lancet into the lancet holder and push down until it is fully seated.
2. Twist o the protective cap until it separates from the lancet.
3. Replace the depth adjustment cap and set the puncture depth to the desired number.
NOTE: THE SHORTER THE SCALE THE SHALLOWER THE PUNC TURE.
4. Pull back the cock ing control until it makes a click, press release but­ton for penetration. If it does not click, the device may have been cocked when the lancet was insert­ed. Please contact local distributor.
Performing Blood Test
About GoodLife
Intended Use
The GoodLife Blood Glucose Monitoring System is designed to quantitatively measure the level of glucose in capillary whole blood by people with diabetes or by healthcare pro­fessionals for monitoring blood glucose at home or in health­care facilities. The device is indicated for professional use and over-the-counter sales.
Principle of the Test
The GoodLife System is an electrochemical biosensor system that measures the amount of electric current pro­duced and displays the result as a blood glucose level.
About the System
The GoodLife System is designed to pursuit the accuracy in blood glucose monitoring to provide you with easy and comfortable testing. The system requires 0.5μL of blood sample and 5 seconds for the test to complete. The GoodLife System consists of: GoodLife Blood Glucose Meter GoodLife Blood Glucose Test Strips(AC, also known as ACH) GoodLife Check Strip GoodLife Glucose Control Solution (optional) Lancing Device (optional) Lancets (optional) These products are intended to be used together to get accurate blood glucose test results. Do not use other test strips or control solutions with your meter.
Important Information
The GoodLife System is intended for in vitro diagnostic
use with capillary whole blood. The system should not be used for diagnosis of diabetes or for testing newborn in­fant (neonatal testing).
CAUTION
1. The user should not take any medical relevance deci-
sion based on test result without rst consulting his or her medical practitioner.
2. Call your doctor immediately if you experience symp-
toms that are not consistent with your blood glucose test results.
3. Severe dehydration or excessive water loss may cause
false, high results. Call your doctor right away if you sus­pect you are suering from dehydration.
4. A sample with large amount of reducing substances
such as triglycerides (>11.3mmol/L), ascorbic acid
(>0.13mmol/L), uric acid (>0.89mmol/L) and xylose (>
3.4mmol/L).
5. A red blood cell count (hematocrit) that is either very
high (over 55%) or very low (under 30%) can cause false result.
6. High altitudes above than 2,750 meter (8,800 feet) may
aect the test results.
7. Temperatures outside the range of 10°C to 40°C (50°F to
104°F) may aect the test results.
NOTE: PLEASE MAKE SURE THAT ALL PRODUCTS LISTED ON THE “CONTENTS” OF THE BOX ARE CONTAINED IN THE
Please read this User Guide before using your GoodLife Blood Glucose Meter (AC-300). If you have any questions or enquiries, please contact us or your local distributor.
Blood Gluc ose Monitoring Syste m
User Guide
User Guide
1. Wash your hands throughly with soap and warm water. Rinse and dry completely. Warm your ngers to increase blood ow.
2. Take out new test strip from vial. Be sure to tightly replace vial cap after taking out test strips. Insert test strip immediately into strip slot as illustrated. The meter turns on automatically.
3. Check that the code number on the meter matches the code on the vial. If the 2 numbers are matched, you may begin blood testing, otherwise consult your local distributor.
9
4. When the symbol flashes, you are ready to perform a test.
5. If the test is done in 2 hours of meal, press button to change the setting from to .
6. Hold the prepared lancing device firmly against the side of your fin­ger. Press the release button. Gently massage your finger to obtain the required blood volume. To perform the test, you need 0.5uL of blood sample resting on your nger. Caution: To avoid the blood borne pathogen transmission, the lancing device is intended only for a single user and should not be shared.
7. Apply the blood sample to the
front aperture of test strip in a way that is comfortable for you. Make sure that the blood drop has satu­rated the Blood Reaction Zone. When blood is applied to the strip, a count down appears on the screen until measurement is com­pleted.
8. Test result will show up in 5 sec-
onds.
9. Record your testing result in the
log sheet, eject the strip from me­ter and discard the used strip and lancet safely in a puncture resis­tant container.
10. The testing range of the meter
is from 1.1 to 33.3 mmol/L. If HI is displayed, your blood glucose result may be higher than 33.3 mmol/L. If LO is displayed, your blood glucose result may be lower than 1.1 mmol/L.
Understanding Your Test Result
Expected values for people without diabetes:
Time of Day Expected Range, Non-diabetes
Source: American Diabetes, Association Position Statement, Diabetes Care Vol.35 (Suppl.1) P.S13 (2012).
Before Meal Less than 5.6 mmol/L
After Meal Less than 7.8 mmol/L
For diabetes patients, please consult your healthcare pro­fessional to nd out your target blood glucose value.
If your blood glucose result seems unusually high or low, or inconsistent with your previous results, check the fol­lowing:
1. Does the code number on the test strip vial match the code number on the me ter?
2. Was the blood sample applied to the test strip immedi­ately after the strip was removed from the vial?
3. Was the size of the blood sample sucient?
4. Was the test strip vial cap tightly sealed?
5. Was the test str ip used before the expiration date?
6. Were the test strips stored away from ex treme tempera­tures or from areas of high humidit y?
Then run a quality control check with your GoodLife Glucose Control Solution and a new test strip. If the control test result is within the acceptable range, review testing procedure and repeat your blood glucose test with a new test strip. If your blood glucose value is still inconsistent with your previous results, contact your doctor immediately for help.
Memory Recall
The GoodLife Blood Glucose Meter can automatically store up to 900 results on both before a meal and after a meal . When recalling the results, each single result appears from the latest to the earliest with time and date.
To recall Results Stored in Memory
1. Turn meter on by press but ton till you hear a beep sound. The first result displayed on the screen is your 30 days average before a meal test result.
2. Press button to view 30 days average after a meal and the single test record from the most recent latest to the oldest.
3. Please press the button for 2 seconds to turn o or put it aside for 3 minutes for auto shut down.
NOTE: ANYTIME IN MEMORY MODE, YOU CAN PRESS BUT­TON UNTIL YOU HEAR THE BE EP TO EXIT AND TURN OFF THE METER.
Data Download (optional)
Data can be transfered to the server or pc by RS232 cable line.
Taking Care of Your Meter
To Replace the Battery
1. Make sure the meter is turned o.
2. Place the meter face down on a at surface..
3. Slide battery compartment door open.
ÌGLAC-3Ç !-Î
4. Remove the old battery and insert new CR2032 battery into the battery compartment. Be sure to align the plus (+) and minus (-) signs correctly.
ÌGLAC-3Ç !-Î
5. Close the battery compartment door. Check to see that your meter is working. If it fails to turn on, the battery may has been inserted incorrectly. Remove the battery and reinsert it correctly.
ÌGLAC-3Ç !-Î
NOTE: EVERY TIME WHEN YOU REPLACE THE BATTERIES, THE METER WILL TURN ON AUTOMATICALLY AND ENTER TO THE TIME/DATE SETTING. PLEASE SET CORRECT TIME AND DATE BEFORE TESTING.
CLEANING
Clean the outside of the meter with a soft cloth, slightly dampened with water. Do not get moisture into the strip slot and data port.
STORAGE AND HANDLING
Keep your meter free of dus t or water. Protect it from extreme temperature and humidit y.
CAUTION
If the product is not used for longer periods of time, please remove the inserted battery in order to prevent damage caused by leaking battery. Please follow all the instructions on the User Guide while operating GoodLife Blood Glucose Meter. HMD BioMedical
AC-300
❹ ❿
Inc. will not be responsible for any impairment occurred from NOT following the instructions.
WARRANTY
HMD BioMedical Inc. warrants to the original purchaser that this instrument will be free of defects in material and workmanship for 5 years from the date of original pur­chase. During the stated 5-year period, HMD shall, at no charge, replace a unit found to be defective with an equiv­alent or current version of the owner’s model.
This warranty is limited to replacement due to defec ts in parts or workmanship. HMD shall not be re quired to re­place any units which malfunction or are damaged due to abuse, accidents, alteration, misuse, neglect, maintenance by other than HMD, or failure to operate the instrument ac­cording to instructions.
POST- SALE SERVICE
If you have questions or request, please contact our service department at
Australia Region
JNS Biomedical Pty. Ltd. service@jnsbiomedical.com.au
Display Messages and Problem-Solving Guide
When any of the following messages appears, there is a problem with your GoodLife Blood Glucose Meter or the way in which you are performing a test. These messages will help you to identify certain problems. If error messages appear that are not listed on the following pages, contact with your local distributor for help.
Display Decription A cti on to Ta ke
Y
Display check
If some parts of the dis­play are not working. Contact your local dis­tributor for help.
Blood glucose result may be higher than
33.3 mmol/L.
Review proper testing procedure and perform a quality check with control solution. Repeat blood test, if “HI” still ap­pears, call your doctor immediately.
Blood glucose result may be lower than 1.1 mmol/L.
Review proper testing procedure and perform a quality check with con­trol solution. Repeat test, if “LO” still appears, call your doctor immediately.
Temperature is above or below the op­erating range of test strips.
The result you have obtained may not be accurate. Move to an area with temperature between 10ºC to 40ºC (50ºF - 104ºF). Do not ar­tificially heat or cool the mete r.
Battery is low.
Change battery immedi­ately.
Test strip un­known or may be damaged.
Perform the test with new test strip.
Test strip is used or test was not per­formed cor­rect ly.
Perform the test with a new test strip and follow the test procedure cor­rect ly.
No respons­es when strip is inserted into the me­ter.
Maybe:
1.Battery is dead.
2.Wrong strip was inser ted.
3.Meter is de­fective.
You have to:
1. Replace battery.
2. Insert the test strip corre ctly.
3. Contact us for help.
No respons­e s w h e n blood sam­ple is applied to the strip.
Maybe:
1.Blood sample is not sucient.
2.Meter is de­fective.
You have to:
1. Repeat test with suf­cient sample.
2. Perform Meter Check by inserting check strip.
System Specication
1. Assay Method: Electrochemical biosensor
2. Test Sample: Fresh Capillary Whole Blood
3. Calibrated Result: Plasma / Serum glucose
4. Sample Size: 0.5 μL
5. Measuring Time: 5 seconds
6. Measuring Range: 1.1 – 33.3 mmol/L
7. Acceptable Hematocrit Range: 30%-55%
8. Operating Temp. Range: 10°C~40°C(50°F~104°F)
9. Operating Relative Humidity: 20% - 80% RH
10 . Memory Capacity: 900 test results with time and
date
11. Result Setting: Before a meal, After a meal and Con­trol solution test setting
12. Average Display: 30 days average
13. Power Supply: CR2032 Battery x 1
14. Battery Life: Approximately 1000 tests
15. Automatic shut-o: In 3 minutes
16. Meter Dimension: 90mm (L) x 45mm (W) x 15mm (H)
17. Weight: Approximate 50g (without battery)
Performance Evaluations
Precision
Tests were carried by trained technicians in the laboratory setting. The venous whole blood from one subject was adjusted to 6 dierent levels. Strips out of a single lot were tested. The results are shown in the following table.
Level No. of te st Mean
(mmol/L)
Within-Run C.V.
(%) I II III
IV V VI
100 100 100 100 100 100
2.3
5.6
6.9
12.0
18.9
29.9
4.6
4.1
2.5
3.6
3.5
2.6
Accuracy
Tests were performed at hospital by healthcare profession­als and diabetic patients. Fresh capillary nger whole blood samples were tested with the GoodLife System; plasma samples from the subjects were tested with YSI Model 2300 Glucose Analyzer as reference. The results are shown in the following table.
Slope 0.93 y-intercept 0.3 mmol/L Correlation Coecient (R) 0.99 Number of tests 200 Range tested 1.8~24.7 mmol/L
Glucose Concentration < 4.2mmol/L Within ± 0.3mmol/L Within ± 0.6mmol/L Within ± 0.8mmol/L 32/38 (84%) 38/38 (100%) 38/38 (100%) Glucose Concentration ≥ 4.2mmol/L Within ± 5 % Within ± 10 % Within ± 15 % Within ± 20 % 86/162 (53%) 138/162 (85%) 159 /162 (98%) 161/162 (99%)
NOTE: THE PRODUCT IS TESTIFIED BY A THIRD PARTY THAT IT DOESN’T INTERFACE WITH OTHER POSSIBLE ELECTRO­MAGNETIC WAVE.
Batch code Temperature limitation / Store at Caution Do not reuse
3K-02-160035 V1.4
Keep away from sunlight
Biological risks
Please consult instructions for use In vitro diagnostic medical device. Use by /Expiry date Serial number Manufacturer Authorised representative in the European com-
munity This product fullls the requirement of directive
98/79/EC in vitro diagnostic medical device The symbol indicating seperate collectionfor
electrical and electronic equipment consists of the crossed-out wheeled bin. When the end-user wishes to discard this product, it must be sent to seperate collection facilities for recovery and recycling. By separating this product from other household-type waste, the volume of waste sent to incinerators or land-fills will be reduced and natural resources will thus be conserved.
Distributed by :
JNS Biomedical Pty. Ltd.
Paramount Centre, Shop 4a, 108 Bourke Street, Melbourne Vic 3000, Australia ABN: 79 163 593 833 service@jnsbiomedical.com.au
HMD BioMedical Inc.
No. 181, Minsheng St., Xinpu Township, Hsinchu 305, Taiwan
FIA Biomed GmbH
Rheiner Strasse 172, D-48282 Emsdetten, Germany
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