Registering medical devices on EUDAMED: operating mode & feedback from a manufacturer

Registering medical devices on EUDAMED: operating mode & feedback from a manufacturer

Legal manufacturers marketing medical devices in Europe have entered the transitional year before Eudamed’s mandatory implementation in January 2026 for registering their products. This webinar provides an opportunity to review the operational procedures and associated standards. It is also an opportunity to get initial feedback from a manufacturer on the publication of these products via…