Accu-Chek Mobile User Manual

252
Explanation of symbols23
On the packaging, on the back of the meter and on the lancing device, you may encounter the symbols shown
below. They have the following meanings:
Consult instructions for use
Caution (refer to accompanying docu-
ments)! Please refer to safety related
notes in the instructions for use accom-
panying this instrument.
Store at
Use by / Expiry date
Use only once
Sterilized using irradiation
Manufacturer
Catalogue number
Lot number
IVD
For in vitro diagnostic use
0088
Blood glucose meter: This product fulls
the requirements of the European Direc-
tive 98/79/EC on in vitro diagnostic med-
ical devices.
0088
Blood glucose meter: This product fulls
the requirements of the European Direc-
tive 1999/5/EC on radio and telecommuni-
cations terminal equipment (R&TTE).
0088
Lancing device and lancet drum: These
products full the requirements of the
European Directive 93/42/EEC on medical
devices.
0088
AST cap: This product fulls the require-
ments of the European Directive 93/42/EEC
on medical devices.
This device complies with Part 15 of the
FCC Rules and with RSS-210 of Industry
Canada.
N20091
The compliance mark indicates that the
product complies with the applicable
standard and establishes a traceable link
between the equipment and the manufac-
turer, importer or their agent responsible
for compliance and for placing it on the
Australian and New Zealand market.
Explanation of symbols23

Accu-Chek Mobile Specifications

General

Measurement Technology	Photometric
Sample Type	Capillary whole blood
Sample Size	0.3 µL
Test Time	5 seconds
Battery Type	2 AAA batteries
Connectivity	USB
Dimensions	121 x 63 x 20 mm
Weight	129 g (with batteries)
Display	LCD
Memory Capacity	2000 results
Measuring Range	0.6 - 33.3 mmol/L
Operating Temperature	10 - 40°C
Operating Humidity	10 to 90% RH
Hematocrit Range	20 to 70%
Test Strip Technology	No test strips required (uses a test cassette)