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Get ready and learn more about the mandatory use of EUDAMED, the European Database on Medical Devices.
Commission Decision (EU) 2025/2371 of 26 November 2025 on the notice regarding the functionality and the fulfilment of the functional specifications of certain electronic systems included in the European Database on Medical Devices declaring the functionality of the first four modules has been published in the OJEU on 27 November 2025.
In accordance with the transitional provisions set out in Regulation (EU) 2024/1860, this publication triggers a transition period of 6 months; therefore, as from 28 May 2026 the Actor, the UDI/Devices, the NBS & Certificates and the Market Surveillance modules are mandatory to use.
Factsheet
Presentations
These presentations aim at giving all concerned actors an overview about their obligations under the Medical Devices Regulations (Regulation (EU) 2017/745 — MDR, and Regulation (EU) 2017/746 — IVDR) and help them to be ready for the mandatory use of the first four EUDAMED modules.
- Introduction and regulatory framework
- Actor module
- UDI/Devices module
- NBs & Certificates module
- Market Surveillance module
Trainings and Other Onboarding Activities
Watch the recordings of the latest EUDAMED webinars:
- Actor module - 28 April 2026 (recording link)
- UDI/Devices module - 5 May 2026 (recording link)
- Notified Bodies & Certificates module - 7 May 2026 (recording link)
- New SS(C)P functionality – 2 July 2026 (recording link)
The material used for EUDAMED training is available in the EUDAMED Information Centre.
