Eudamed: New Dates, Constant Challenges But Light At The End Of The Tunnel

The European medical device database, Eudamed, is arguably the missing lynchpin in the implementation of the EU’s Medical Device and IVD Regulations. Medtech Insight spoke with Lionel Tussau of atrify to discover what companies need to know now and how actors should be preparing.

Timeline years 2025 blue pin
• Source: Olivier Le Moal / Alamy Stock Photo

Moves are afoot which should lead to the Eudamed medical device database being substantially fully functional by the end of 2024, resulting in mandatory use of all six modules around mid-2025, although with caveats for the UDI (Unique Device Identification) and certificate modules. 

That is according to the latest news on Eudamed, which is being updated to fit with the Medical Device and IVD Regulations’ requirements. 

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