The European Commission shared a time line for the planning of the outstanding phased releases of the long awaited medical device database in June 2022. Originally scheduled to go live in May 2020, the database aims to register every medical device authorized, to be used across the 27-member European Union. The new time line suggests that the database will achieve full functionality by the second quarter of 2024. Eudamed’s use will be mandatory, as regards obligations and requirements related to Actors, Vigilance, Clinical Investigation & Performance Studies and Market Surveillance modules in the fourth quarter of 2024.