The 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 (referred to in Article 34(1) of Regulation (EU) 2017/745) declaring the functionality of the first four modules was published in the OJEU of 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, mandatory use of the first four modules of EUDAMED (listed below) will commence from 28 May 2026,
- Actor registration
- UDI/Devices registration
- Notified Bodies & Certificates
- Market Surveillance
Source: European commission