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Accu-Chek Mobile User Manual

Accu-Chek Mobile
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Testing and storage conditions15
NOTICE:
Changes or modications made to this equipment not
expressly approved by Roche Diagnostics GmbH,
Germany may void the FCC authorization to operate
this equipment.
Classication with respect to U.S. telecommunication
requirements (47CFR §15.105)
NOTE:
This equipment has been tested and found to comply
with the limits for a Class B digital device, pursuant to
Part 15 of the FCC Rules. These limits are designed to
provide reasonable protection against harmful interfer-
ence in a residential installation. This equipment gen-
erates, uses and can radiate radio frequency energy
and, if not installed and used in accordance with the
instructions, may cause harmful interference to radio
communications. However, there is no guarantee that
interference will not occur in a particular installation. If
this equipment does cause harmful interference to
radio or television reception, which can be determined
by turning the equipment off and on, the user is en-
couraged to try to correct the interference by one or
more of the following measures:
Reorient or relocate the receiving antenna.
Increase the separation between the equipment and
receiver.
Connect the equipment into an outlet on a circuit
different from that to which the receiver is con-
nected.
Consult the dealer or an experienced radio/TV tech-
nician for help.
Classication with respect to the Canadian telecom-
munication requirements
NOTICE:
This Class B digital apparatus complies with Canadian
ICES-003.

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Accu-Chek Mobile Specifications

General IconGeneral
Measurement TechnologyPhotometric
Sample TypeCapillary whole blood
Sample Size0.3 µL
Test Time5 seconds
Battery Type2 AAA batteries
ConnectivityUSB
Dimensions121 x 63 x 20 mm
Weight129 g (with batteries)
DisplayLCD
Memory Capacity2000 results
Measuring Range0.6 - 33.3 mmol/L
Operating Temperature10 - 40°C
Operating Humidity10 to 90% RH
Hematocrit Range20 to 70%
Test Strip TechnologyNo test strips required (uses a test cassette)

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