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:

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Fabricants d'implants
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Thieme eRef integration
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Branch office Bad Homburg:
Werner-Reimers-Straße 2-4
D-61352 Bad Homburg
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