27
Instructions for Use
Copyright © 2020
DocumentID
Version
Date
27 / 33
Fiagon GmbH
DOC-19-00169 2
08-2020
EN / US
Preparation for disposal
If the device should be finally shut down at the end of its lifetime it is necessary to contact the manufacturer or
the local representative of the company in your country to get the valid instructions needed for disposal of the
device in compliance with the standards applying. If components of the device should be disposed it is also
necessary to contact the manufacturer or the local representative of the company in your country to get the valid
instructions needed for disposal of these components in compliance with the standards applying.
Technical description
12.1. Conformity
The Navigation System was found to be in compliance with the European Medical device directive and has been
affixed with the CE marking. Therefore, it is compliant with the following directive:
MDD 93/42/EEC
12.2. Manufacturer
The manufacturer acts in compliance with international and national standards and laws. Information about the
compliance can be provided on request. Please contact your regional consultant or contact Fiagon using the
following contact details :
Fiagon GmbH
Neuendorfstrasse 23b
16761 Hennigsdorf
Germany
Phone: +49 3302 201 21 10
Fax: +49 3302 201 21 15
