cobas Accutrend Plus Instrucciones De Uso página 4

©2011, 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 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, ACCU-CHEK MULTICLIX, ACCUTREND, COBAS and SAFE-T-PRO are trademarks
of Roche.
All other trademarks are the property of their respective owners.
This instrument has been constructed and tested in accordance with EN 61010-1 ("Safety
requirements for electrical equipment for measurement, control and laboratory use; Part 1:
General requirements") and left our factory in a safe condition.
To ensure that this remains so and to ensure safe operation the user must observe the instruc-
tions and warnings given in this manual.
Installation, use and maintenance of the Accutrend Plus meter lie in the full responsibility of the
user.
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
manual accompanying this instrument.
Temperature limitation (Store at)
Use by
Manufacturer
Batch code/ Lot number
Catalogue number
In vitro diagnostic medical device
This product fulfills the requirements of the European Directive 98/79/EC on in vitro
0123
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)
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