
4
© 2012 Roche Diagnostics GmbH. 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 editorial 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, COAGUCHEK and SAFE-T-PRO are trademarks of Roche.
All other trademarks are the property of their respective owners.
On the packaging and on the identification plate of the instrument you may encounter the
following symbols, shown here with their meaning:
Caution, consult accompanying documents. Refer to safety-related notes in the
instructions for use accompanying this product.
Temperature limitation (Store at)
Use by
Manufacturer
Batch code/ Lot number
Catalog number
In vitro diagnostic medical device
This product fulfills the requirements of the European Directive 98/79/EC on in vitro
diagnostic medical devices.
Consult instructions for use
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).
LOT
IVD
Commentaires sur ces manuels