MBG10-6/0741 Blood Glucose Monitor Instruction Manual Please read all instructions carefully and retain for future use
Know your Device Principle of Operation Intended use of the equipment Limitation of Use Important Safety Information and precautions Preparation 3 4 5 Introduction for Use Before Use, Setting the monitor Delete Memory Instruction for Use About Color Bars Physical and Performance Deterioration Alternative Site Testing 6 7 8 10 11 Care and Maintenance Units of Measure 12 13 Troubleshooting 14 EMC Declaration FCC Compliance 16 19 Specifications 20 Analysis 21 Additional Glucose Test Strips Warra
KNOW YOUR DEVICE Principle of Operation Testing with the Blood Glucose Monitoring is based on the measurement of electrical currents generated by the reaction of glucose with the reagent of the strip. The blood glucose monitoring system measures the current and converts it to the corresponding blood glucose level. The strength of the current produced by the reaction depends on the amount of glucose in the blood sample.
Important Safety Information and Precautions • Misuse of the blood glucose monitoring system can cause electrocution, burns, fire, and other hazards. • The glucose monitor and lancing device are for single patient use. Do not use either item on multiple patients. • Do not share the monitor or lancing device with anyone, including other family members. • Do not place the blood glucose monitoring system in or near liquid.
PACKAGE CONTENTS • Blood Glucose Meter • 10 Test Strips and 10 Lancets • Storage Case and Log Book • Lancet Device • Instruction Manual PARTS OF MONITOR Date Time Average Range Memory CTL Symbol Measurement Unit Low Battery Alarm Clock Blood Sample SET Button MEM Button Eject Button Display monitor’s date Display monitor’s time Display the 7/14/21/28/60/90 days average Appears when checking past test result Appears when doing a control test and indicates that the result will not be stored in the memory Ap
Before Use • Severe dehydration and excessive water loss may cause inaccurate results. If you believe you are suffering from severe dehydration, consult your healthcare professional immediately. • Inaccurate results may occur in severely hypotensive individuals or patients who are in shock. Test results that are lower than actual values may occur in individuals who are in a hyperglycemic-hyperosmolar state, with or without ketosis. Critically ill patients should not be tested with blood glucose monitor.
Delete Memory Delete Memory When “dEL” is flashing and a “ ” symbol appears on the screen, press M to delete all the memory. “___” will flash three times and screen will auto off. Setting of Alarm You may set up any or all of the alarms (1 - 4). When “dEL” is flashing and a “ set the alarm. ” symbol appears on the screen, press S to When the “OFF” or “On” and “ ” symbols appear on the screen, press M to turn on or off the first alarm. Press M to select on, press S to set the hour.
Before Taking Test for Blood Glucose To reduce the chance of infection: • Choose a clean, dry work surface. • Never share a lancing device or lancet with other person. • Always use a new and sterile lancet. • Always use a new test strip. the test strip is for single use only. • Avoid getting lotion, oils, dirt, or debris in or on the lancet and lancing device. A sample may be obtained from the finger by the following steps: 1. Wash your hands all the time, before the following steps. 2.
1. Obtain a blood sample Press the lancing device against the site to be lanced. Press the release button to puncture the site. Squeeze your finger until a drop of blood forms. Wipe away the first blood drop and squeeze until a second small blood drops forms. 2. Apply the blood sample to the test strip Quickly apply the blood sample to the absorbent hole of the test strip. Make sure the confirmation window of the test strip is completely filled with the blood sample.
About the Color Bars On the panel of the Blood Glucose Monitor (MBG10-6/0741), there is a color bar. It is used for indicating blood glucose value range. The Color Bar’s image is showing in picture (c) as below.
PHYSICAL AND PERFORMANCE DETERIORATION If you start experience one of the following, Stop using and contact local customer services or the place of purchase for assistance. 1. The device does not work. 2. Discoloration of the monitor casing or lancing device; for example, it is difficult to read the labeling information. 3. Corrosion, crazing (fine cracks), embrittlement, and/or cracking of the monitor casing or lancing device.
Compare Glucose Monitor Test Result with Laboratory Results The results obtained from the glucose monitor are plasma-calibrated. The result you obtain from your glucose monitor may differ somewhat from your laboratory results due to normal variation. Monitor results can be affected by factors and conditions that do not affect laboratory results in the same way. To make an accurate comparison between monitor and laboratory results, follow the guidelines below.
INTERNATIONAL BLOOD GLUCOSE UNITS OF MEASURE Country Unit of Measure Used Country Unit of Measure Used Algeria Argentina Austria Bahrain Bangladesh Belgium Brazil Caribbean Countries Chile Colombia Ecuador Egypt France Georgia Greece India Indonesia Israel Italy Japan Jordan Korea Kuwait Lebanon Luxembourg Mexico Oman Peru Philippines Poland Portugal Saudi Arabia Spain Syria Taiwan Thailand Tunisia Turkey United Arab Emirates (UAE) United States Uruguay Venezuela Yemen mg/dL mg/dL mg/dL mg/dL mg/dL mg/
If you follow the recommended action but the problem persists, or error messages other than the ones below appear, please call your local customer service. Do not attempt to repair the monitor by yourself and never try to disassemble the monitor under any circumstances. Display Messages Message What It Means Blood glucose level is lower than 20mg/dL (1.1mmol/L). What To Do The message indicates very low blood glucose. Consult with your healthcare professional. Blood glucose level is than600mg/dL (33.
(continued) Problem Display remains blank after the test strip has been inserted into the monitor. Test results are inconsistent. Possible Causes 1. Battery power is too low for use. 2. Too much time has passed between inserting the test strip and performing the test. 3. Test strip has not been fully inserted into the monitor. 1. Not enough sample in the test strip. 2. Test strip has expired. 3.
ELECTROMAGNETIC COMPATIBILITY INFORMATION Table 1 For all ME EQUIPMENT and ME SYSTEMS Guidance and manufacture’s declaration - electromagnetic emissions This device is intended for use in the electromagnetic environment specified below. The customer or the user of this device should assure that it is used in such an environment.
Table 2 For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING Guidance and manufacturer’s declaration - electromagnetic immunity This device is intended for use in the electromagnetic environment specified below. The customer or the user of this device should assure that it is used in such an environment.
Table 3 For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and this device This device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
This device complies with Part 15 of the FCC rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Caution: Changes or modifications to this device not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.
Model MBG10-6/0741 Product Size 110mm (L) x 52mm (W) x 20.5mm (D) Measuring Method Amperometric technology using glucose dehydrogenase Result Range 20 mg/dL ~600 mg/dL (1.1 mmol/L ~33.3mmol/L) Power DC3V Storage Condition - Monitor -4°F～131° F (-20°C～55°C); Humidity 10%～80%RH Storage Condition – Test Strips 39.2°F～86°F (4°C～30°C), Humidity 10% ～ 85%RH Operating Condition 50°F～104°F (10°C～40°C) , 25%RH～80%RH Blood Source Fresh capillary whole blood Blood Volume Minimum 0.
If you are taking acetaminophen containing drugs (Tylenol and other medicines containing acetaminophen, blood concentrations >5 mg/dL) or Vitamin C (ascorbic acid, blood concentrations >4 mg/dL) at doses higher than recommended, these may interfere with your glucose meter and cause you to get inaccurate results with this system. System Accuracy: The System was tested on 350 capillary blood samples, and this is the accuracy in the hands of lay users.
ADDITIONAL GLUCOSE TEST STRIPS To buy additional Glucose-Test Strips, please visit www.nuvomed.us WARRANTY DURATION: All materials and workmanship are warranted to the original consumer purchaser for a period of ninety (90) days from the original purchase date. WARRANTY COVERAGE: This product is warranted against defective materials or workmanship.
no representative or person is authorized to assume for manufacturer any other liability in connection with the sale of our products. There shall be no claims for defects or failure under any theory of tort, contractor commercial law including but not limited to, negligence, gross negligence, strict liability, breach of warranty and breach of contract. Under no circumstances will Manufacturer’s / Distributor’s maximum liability exceed the retail value of the product. Manufactured by ANDON HEALTH CO., LTD.
