EU Advisory Body
Appears in 1 story · Last updated May 28, 2026
As of May 2026: Sets EUDAMED registration guidance for member states
Until today, registering a pacemaker, hip implant, or COVID test for sale in Europe meant filing paperwork with each of the 27 national regulators. From May 28, 2026, there is one database. Every medical device and in vitro diagnostic sold in the EU must be entered into EUDAMED, the centralized European registry, before it reaches a hospital shelf.
Updated May 28
No stories match your search
Try a different keyword
How would you like to describe your experience with the app today?
