Accu-Chek Inform II User Manual

08424705001 (01) 2017-04 USA • Accu-Chek Inform II Operator’s Manual Version 6
On the packaging, on the identification plate of the meter, the battery pack, the base unit, or the code key
reader you may encounter the following symbols, shown here with their meaning:
On meters with WLAN capability:
For other WLAN certifications, see label on bottom of battery compartment.
Caution, consult accompanying documents. Refer to safety-related notes in the instructions
for use accompanying this product.
Temperature limitation (Store at)
Manufacturer
Date of manufacture
Catalog number
In vitro diagnostic medical device
Global Trade Item Number
Serial Number
The system fulfills the Canadian and U.S. safety requirements (UL LISTED, in accordance
with UL 61010-1 and CAN/CSA-C22.2 No. 61010-1).
Power supply connection (Base Unit Light)
Power supply connection (Base Unit)
Rx only
Caution: Federal law restricts this device to sale by or on the order of a physician
This device complies with Part 15 of the FCC Rules and with RSS-210 of Industry Canada.
The compliance mark indicates that the product complies with the applicable standard and
establishes a traceable link between the equipment and the manufacturer, importer or their
agent responsible for compliance and for placing it on the Australian and New Zealand
market.
IVD
SN
7.5V 1.
7
12V 1,25
A

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