We at Trumpf Medical are constantly developing our products.
Therefore, we reserve the right to make changes to the format, 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 + Co. KG.
TRUMPF Medizin Systeme GmbH + Co. KG expressly reserves all rights under copyright law.
Within the bounds of the legal requirements, the manufacturer is responsible for the technical safety characteristics
of this apparatus only 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.
Valid for CE marked products (see model plate):
–
CE mark:
This is a Class I medical device according to the Council Directive 93/42/EEC
concerning medical devices and is compliant with the Directive version currently in force at
the time of product sale including its changes.
–
Conformity:
The manufacturer declares the conformity of this product with the essential
requirements of the Council Directive 93/42/EEC concerning medical devices according
to Annex I, as well as the implementation of an assessment procedure required for Class I
product conformity under Annex VII and documents this with the CE mark.
Manufacturer and distributor
TRUMPF Medizin Systeme GmbH + Co. KG
Carl–Zeiss–Straße 7–9
07318 Saalfeld
Germany
www.trumpfmedical.com
Phone
+49 3671 586–0
Fax
+49 3671 586–41165
Technical customer service
Phone
+49 3671 586–41911
Fax
+49 3671 586–41175
Translation of the original German instruction manual
Revision level: 02/11/2017
Document number: 4990113_030_01
© TRUMPF Medizin Systeme GmbH + Co. KG
