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Accu-Chek Inform II User Manual

Accu-Chek Inform II
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Supplement for Enhanced Workflows • E
233
08424705001 (01) 2017-04 USA • Accu-Chek Inform II Operator’s Manual Version 6
3 Enter or select the patient ID. For more details see
pages 51 - 55.
4 Perform the test. For more details see pages 58 - 61.
123
456
789
A-O0
Patient ID
12:48 pm
03/17/17
ABCDE
F GHI J
KLMNO
P-Z 123
Patient ID
123456789
12:48 pm
03/17/17
D-503: Patient ID:
123456789
Name:
Mary-Jane Miller
DOB: 12/03/56
Is this correct?
Patient Confi rmation
Patient Test
Patient 123456789
Strip L
ot 545794
12:48 pm
03/17/17
DOB: 12/05/70
The test strips should be used immediately after remov-
ing them from the test strip vial (see package insert).
However, where this is not possible due to an altered
workflow (example: Isolation Room Workflow), studies
show that the test strips remain stable for 3 minutes
between removing them from the vial and applying a
blood sample.

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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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