This is a class I medical product according to Annex IX of the COUNCIL DIRECTIVE 93/42/EEC concerning
medical devices (MDD) of 14 June 1993.
The manufacturer declares that the essential requirements as stated in Annex I, MDD have been fulfilled, and
that the conformity assessment procedure required for class I products has been performed according to Annex
VII, MDD. This is documented by the CE sign.
We are constantly working on further developments.
Therefore, please understand that we must reserve the right to change the scope of the delivery in respect of
the form, equipment and technology at any time.
Reprinting, copying or translating this document, in whole or in part, is forbidden without the express written
permission of TRUMPF Medizin Systeme GmbH.
All rights under the copyright laws are expressly reserved by TRUMPF Medizin Systeme GmbH.
Within the bounds of the legal requirements, the manufacturer is only then responsible for the technical safety
characteristics of this apparatus if the maintenance, repairs and modifications to this apparatus are performed
by him or by someone appointed by him and in accordance with his instructions.
TRUMPF Medizin Systeme GmbH
Postfach 24 44
D-07310 Saalfeld, Germany
TRUMPF Medizin Systeme GmbH
Carl-Zeiss-Straße 5
D-07318 Saalfeld, Germany
Distribution Telephone +49 3671 586-0
Fax +49 3671 586-166
Technical
Customer Service
Telephone +49 3671 586-172
+49 3671 586-176
Fax +49 3671 586-175
© 09/07 TRUMPF Medizin Systeme GmbH
To Next Page
Loading...
