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Accu-Chek Inform II Guide

Accu-Chek Inform II
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Page 29 of 39
In-service plan for blood glucose testing
ACCU-CHEK Inform II System Test
Name:
ID#:
Date: Unit:
Mark “T” if the statement is True and “F” if the statement is False.
T F
1. Before running a patient test, you must be sure the test strip lot number on the test
strip vial corresponds to the test strip lot number displayed in the
ACCU-CHEK Inform II meter.
2. If “Quality Control is Due” or “QC Due Immediately” appears in the display, you
should run controls and make sure that the results are in range before proceeding
to do a patient test.
3. The ACCU-CHEK Inform II system cannot record operator or patient
ID information.
4. Personal protection equipment must be worn when performing blood glucose
or glucose control testing and when cleaning and disinfecting the ACCU-CHEK
Inform II system.
5. The six-digit number on the meter screen needs to match the number on the test
strip vial you are using.
6. The test strip is placed in the test strip slot with the yellow target area or test
window facing up and the end with the gold bars inserted into the meter.
7. The proper site for the nger puncture is on the side of the ngertip.
8. The test will start when the appropriate amount of sample is applied to the
ACCU-CHEK Inform II test strip, about 0.6 μL.
9. Glucose control solutions do not have to be dated when rst opened.
10. Only capillary whole blood samples should be used when testing with the
ACCU-CHEK Inform II meter and ACCU-CHEK Inform II test strips.
11. The ACCU-CHEK Inform II meter should be docked in the base unit when not
in use.
12. The ACCU-CHEK Inform II meter uses a rechargeable battery.
13. You should touch and hold the drop of blood to the front edge of the
ACCU-CHEK Inform II test strip.
14. Does the meter system detect if there is enough blood sample prior to running the
blood glucose test?

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Accu-Chek Inform II Specifications

General IconGeneral
Sample Size0.6 µL
Test Time5 seconds
Memory Capacity1000 test results
DisplayLCD
Measurement Range10 to 600 mg/dL
ConnectivityInfrared
Sample TypeCapillary whole blood
Operating Temperature16 to 32°C (61 to 90°F)
Relative Humidity10 to 90% non-condensing

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