OverviewEUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746…Actors registrationThe Actor registration is the first of the six EUDAMED modules.UDI/Devices registrationRegulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices introduce an EU device identification…Notified Bodies and CertificatesRegulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) establish that Notified…Getting ready Learning material for EUDAMED onboarding. Prepare confidently for the mandatory use of the system. Latest updatesNews announcement27 November 2025The EUDAMED four first modules will be mandatory to use as from 28 May 20261 min readNews announcement10 November 2025Coordinated assessment for clinical investigations: a call for expression of interest1 min readNews announcement5 September 2025Registration - EUDAMED Workshops: 8 October 2025, Rome, Italy - 3 December 2025, Brussels, Belgium1 min readNews announcement23 May 2025Presentations available - EUDAMED Workshop – 21 May 2025 - Stuttgart, Germany1 min readSee all HighlightsThe EUDAMED Information Centre is the central point of support for EUDAMED users, presenting action steps and process logic from a wide range of documentationThe UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI systemFactsheet on MDR requirements for Transparency and Public Information Events 03Dec2025Training and workshopsEUDAMED Workshops: 8 October 2025, Rome, Italy - 3 December 2025, Brussels, Belgium21May2025Training and workshopsEUDAMED Workshop – 21 May 2025 - Stuttgart, GermanyStuttgard, Germany DocumentsEventsPublications
OverviewEUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746…
UDI/Devices registrationRegulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices introduce an EU device identification…
Notified Bodies and CertificatesRegulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) establish that Notified…
Getting ready Learning material for EUDAMED onboarding. Prepare confidently for the mandatory use of the system.
News announcement27 November 2025The EUDAMED four first modules will be mandatory to use as from 28 May 20261 min read
News announcement10 November 2025Coordinated assessment for clinical investigations: a call for expression of interest1 min read
News announcement5 September 2025Registration - EUDAMED Workshops: 8 October 2025, Rome, Italy - 3 December 2025, Brussels, Belgium1 min read
News announcement23 May 2025Presentations available - EUDAMED Workshop – 21 May 2025 - Stuttgart, Germany1 min read
The EUDAMED Information Centre is the central point of support for EUDAMED users, presenting action steps and process logic from a wide range of documentation
The UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI system
03Dec2025Training and workshopsEUDAMED Workshops: 8 October 2025, Rome, Italy - 3 December 2025, Brussels, Belgium
