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GMED designated under Regulation (EU) 2017/745 on medical devices

BySylvie

GMED official publication on linkedin:

GMED (CE 0459) has been designated as a Notified Body under the Regulation (EU) 2017/745 by the French National Agency for Medicines and Health Products Safety (ANSM).

Equipped with this designation since July 8 2020, GMED has mobilized its teams to offer manufacturers with certification services according to the Regulation (EU) 2017/745 for a field of medical device categories among the broadest.

Read the full communication: https://lnkd.in/datrRVahttps://www.linkedin.com/posts/gmed-north-america_notifiedbody-cemarking-mdr-activity-6686532474765352960-_3V-

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Brexit – rules for Medical Devices if no deal.

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