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Accu-Chek Inform II User Manual

Accu-Chek Inform II
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Introduction • 1
21
08424705001 (01) 2017-04 USA • Accu-Chek Inform II Operator’s Manual Version 6
Disposal of the system
Product safety Observe the following information to ensure product
safety:
The system is suitable for continuous operation.
The system is not protected against the harmful
ingress of fluids (IP X0 rating according to
IEC 60529).
WARNING
Avoidance of electrical shock, fire, and explosions
Only use Roche original accessories (cables, power
supply units, battery packs, and spare parts). Third-
party cables, power supply units, and battery packs
can cause the battery pack to explode or the meter to
become damaged.
Do not use loose power sockets or damaged power
supply units, cables, plugs, or battery packs.
Do not short circuit the power supply unit, the base
unit charging contacts, or the battery pack.
Do not drop the Accu-Chek Inform II meter, the power
supply unit, or the battery pack and protect these
against shaking and vibrations.
WARNING
Infection by a potentially biohazardous instrument
The Accu-Chek Inform II system or its components must
be treated as potentially biohazardous waste. Decontam-
ination (i.e., a combination of processes including clean-
ing, disinfection and/or sterilization) is required before
reuse, recycling, or disposal.
Dispose of the system or its components according to the
appropriate local regulations or your facility policy. For
more information, contact Accu-Chek Customer Care.

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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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