MDR (Medical Device Regulation)

As of 25.5.2017, the new European Medical Device Regulation MDR came into force. It defines from now on the requirements for the conformity assessment of medical devices and combines and replaces two previously independent medical device guidelines. As an European regulation, as opposed to European directives, the Medical Device Regulation must be applied within a period of 3 years as a European supranational law.

 The timeline of mediCAD Hectec is as follows:

MDR Screen

EndoProthetikZentrum
Certification with EndoDok®
Endo
Fabricants d'implants
World's largest database
Implant
Thieme eRef integration
eRef integrated in mediCAD® 3D
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Directions to mediCAD

Headquarter
mediCAD Hectec GmbH
Opalstr. 54
D-84032 Altdorf/Landshut
Germany
Phone: +49 871 330203 0
Fax: +49 871 330 203 99
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Branch office Bad Homburg:
Werner-Reimers-Straße 2-4
D-61352 Bad Homburg
Germany
Phone: +49 871 330203 0

Subsidiary USA:
mediCAD US, Inc.
191 Peachtree St. NE,
Suite 3720 Atlanta,
GA 30303, USA
Phone: +1 470 3441215
Mobile: +1 404 5482012