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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
Implant Manufacturers
World's largest database
Endo
Thieme eRef integration
eRef integrated in mediCAD® 3D
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Headquarter
mediCAD Hectec GmbH
Opalstr. 54
84032 Altdorf/Landshut
Germany

Phone: +49 871 330 203 0
Fax: +49 871 330 203 99
E-Mail: This email address is being protected from spambots. You need JavaScript enabled to view it.
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Branch office Bad Homburg:
mediCAD Hectec GmbH
Werner-Reimers-Straße 2-4
D-61352 Bad Homburg
Germany

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