6 User manual for medifa 5000 operating table Version 2.1
Important information
Version Date Reason or modification of publication
1.0 09/2014 First edition
2.0 09/2018 Layout, content
2.1 05/2021 MDR adjustment
1. Important information
1.1 Revision history
1.2 CE label
This product is a Class 1 medical product according to the Ordinance (EU) 2017/745 on medical products and
complies with the prevailing version of this ordinance at the time of its introduction on the market.
1.3 Conformity
The manufacturer declares the conformity of this product with the essential safety and performance require-
ments according to Medical Device Regulations in Annexe I as well as the implementation of the technical
documentation according to Annexe II and declares conformity by means of an EU Declaration of Conformity
according to Annexe IV.
1.4 Manufacturer and distributor
medifa GmbH & Co. KG
Industriestraße 5
57413 Finnentrop
Germany
Telephone no.: +49 2721 7177-0
Service hotline: +49 2721 7177 410
Fax +49 2721 7177-255
info@medifa.com
www.medifa.com
1.5 Copyright statement
This user manual including all figures is subject to copyright. The transmission and reproduction of this docu-
ment as well as the exploitation and communication of its contents are - unless expressly permitted - prohibited.
Contraventions shall impose an obligation to compensation for damages. All rights reserved in case of a patent
grant or utility model registration.
We are constantly working on the further development of our products. Please understand that we must reserve
the right to change the scope of delivery in shape, equipment and technology at any time.
Reproduction, duplication or translation of the original user manual, even in part, is not permitted without writ-
ten consent from medifa.
All rights according to the copyright law are expressly reserved by medifa. medifa shall only be responsible for
the safety-related properties of this device within the framework of the legal regulations if maintenance, servic-
ing and changes to this device are carried out by medifa itself or a representative in accordance with instructions.
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