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The EU MDR was officially announced on May 5, 2017 and will come into effect on May 25, 2017.

This MDR also contains guidelines for the current Medical Device Directive (MDD) (93/42 / EEC) and active implantable medical devices (90/385 / EEC) in the EU.

The medical device manufacturer has a three-year (until May 26, 2020) transition period to meet MDR requirements.

For certain devices, the completion period may be extended by May 26, 2024 if special requirements are met.


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