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©2014, Roche Diagnostics. All rights reserved.
The contents of this document, including all graphics, are the property of Roche Diagnostics. Information in
this document is subject to change without notice. Roche Diagnostics shall not be liable for technical or
edi torial errors or omissions contained herein. No part of this document may be reproduced or transmitted in
any form or by any means, electronic or mechanical, for any purpose, without the express written permission
of Roche Diagnostics.
Please send questions or comments about this manual to your local Roche representative.
ACCU-CHEK, ACCU-CHEK INFORM and COBAS are trademarks of Roche.
All other trademarks are the property of their respective owners.
The Wi-Fi CERTIFIED Logo is a certification mark of the Wi-Fi Alliance.
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:
Caution, consult accompanying documents. Refer to safety-related notes in the instruction
for use accompanying this instrument.
Temperature limitation (Store at)
Manufacturer
Catalog number
IVD
In vitro diagnostic medical device
The system fulfills the Canadian and U.S. safety requirements (UL LISTED, in accordance
with UL 61010A-1:02 and CAN/CSA-C22.2 No. 61010-1-04).
7.5V
1.7A
Power supply connection
On meters with WLAN capability:
This device complies with Part 15 of the FCC Rules and with RSS-210 of Industry Canada.
For other WLAN certifications, see label on bottom of battery compartment and list included in meter kit.
Содержание Inform 2
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