Accu-Chek Inform II User Manual

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08424705001 (01) 2017-04 USA • Accu-Chek Inform II Operator’s Manual Version 6
Measurement Flow
Comments required* 0: optional
1: out of range
2: required
3: disabled
0NY
Comments requirement level: if out of…
(only valid if Comments required = 1)*
0: normal range
1: critical range
2: reportable range
3: measurement range
0NY
Custom comments* 0: disabled
1: enabled
1NY
* Does not apply to QC measurement workflow
Control lot verification 0: display only
1: yes / no confirmation
2: prompt for entry
3: scan only
1YY
Control result display 0: value (numeric)
1: PASS / FAIL
0NY
Critical range display 0: value (numeric)
1: HI / LO
0NY
Critical range HI limit 10 – 600 mg/dL
0.6 – 33.3 mmol/L
600 mg/dL
33.3 mmol/L
YY
Critical range LO limit 10 – 600 mg/dL
0.6 – 33.3 mmol/L
10mg/dL
0.6 mmol/L
YY
Critical range message enabled Whether to display the
out-of-critical range
warning message (1) or
not (0)
1NY
Critical range text 0 – 100 characters “Out of
Critical
Range”
NY
Normal range HI limit 10 – 600 mg/dL
0.6 – 33.3 mmol/L
600 mg/dL
33.3 mmol/L
YY
Normal range LO limit 10 – 600 mg/dL
0.6 – 33.3 mmol/L
10mg/dL
0.6 mmol/L
YY
STAT tests allowed 0: no
1: yes
0YY
Number of STAT tests allowed 0 – 9 9 Y Y
Reportable range HI limit 10 – 600 mg/dL
0.6 – 33.3 mmol/L
600 mg/dL
33.3 mmol/L
YY
Reportable range LO limit 10 – 600 mg/dL
0.6 – 33.3 mmol/L
10mg/dL
0.6 mmol/L
YY
Subject/Attribute Range Default Device DMS

Accu-Chek Inform II Specifications

General

Sample Size	0.6 µL
Test Time	5 seconds
Memory Capacity	1000 test results
Display	LCD
Measurement Range	10 to 600 mg/dL
Connectivity	Infrared
Sample Type	Capillary whole blood
Operating Temperature	16 to 32°C (61 to 90°F)
Relative Humidity	10 to 90% non-condensing