Trumpf TruSystem 7000 Instruction Manual page 2

Translation of the original German instruction manual
CE mark/Conformity: 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. The manufacturer declares the conformity of this product with
the essential requirements of the Council Directive 93/42/EEC concerning medical devices
according to Appendix I, as well as the implementation of an assessment procedure required
for Class I product conformity under Appendix VII and documents this with the CE mark.
ETL mark: Intertek tested the product for the USA and Canada. ETL classification regarding risk
of electric shock and fire, as well as mechanical hazard in accordance with ULSTD 60601-1;
CAN/CSA STD C22.2 NO.601.1.
Manufacturer and distributor
Sales and Technical Customer
Service
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.
© TRUMPF Medizin Systeme GmbH + Co. KG
TRUMPF Medizin Systeme GmbH + Co. KG
Carl–Zeiss–Straße 7–9
07318 Saalfeld
Germany
www.trumpfmedical.com
Telephone +49 3671 586–41911
Fax +49 3671 586–41175
Email Service.wwo@trumpfmedical.com
TRUMPF Medical Systems, Inc.
1046 LeGrand Blvd.
Charleston, SC 29492
United States
Telephone +1 888 474 9360
Revision level: 24/11/2016
Document number: 4990043_030_00