EUDAMED New
Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) introduce the European database for medical devices (EUDAMED) with Art. 33 MDR and Art. 30 IVDR. This is intended to increase transparency by improving access to information for the public and for healthcare professionals. The modules registration of economic operators, UDI/medical device registration, notified bodies and certificates must be used by economic operators (manufacturers, authorised representatives, importers, manufacturers of systems and procedure packs) and notified bodies from 28th May 2026.
The European Commission is offering free webinars to prepare economic operators and notified bodies for the mandatory use.
The following dates are planned for the respective modules:
- Registration of economic operators: 28th April 2026, from 9:00 to 18:00
- UDI/Medical Device Registration: 05th May 2026, from 9:00 to 18:00
- Notified bodies & certificates: 07th May 2026, from 9:00 to 18:00
The links to the webinars are here They will be activated shortly before the individual webinars.
Further information on EUDAMED including training material from the European Commission can be found here.
Further information on EUDAMED is also available on the BASG website website.
