Kommisjonsbeslutning (EU) 2025/2371 av 26. november 2025 om meddelelse vedrørende funksjonalitet og oppfyllelse av de funksjonelle spesifikasjoner til visse elektroniske systemer inkludert i den europeiske databasen for medisinsk utstyr referert til i artikkel 34(1) i europaparlaments- og rådsforordning (EU) 2017/745
Medisinsk utstyrsforordning 2017: funksjonsspesifikasjoner for Eudamed
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 of the European Parliament and of the Council
Kommisjonsbeslutning publisert i EU-tidende 27.11.2025
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(fra kommisjonsbeslutningen)
(1) According to Article 33(1) of Regulation (EU) 2017/745 and Article 30(1) of Regulation (EU) 2017/746 of the European Parliament and of the Council (2), the Commission is to set up, maintain and manage the European Database on Medical Devices (Eudamed). Eudamed is to include the electronic systems listed in Article 33(2) of Regulation (EU) 2017/745 and Article 30(2) of Regulation (EU) 2017/746.
(2) On 15 December 2022, the Commission published the latest consolidated version of the functional specifications of Eudamed (version 7.2) (3), which it had drawn up in collaboration with the Medical Device Coordination Group (‘MDCG’) in accordance with Article 34(1) of Regulation (EU) 2017/745.
(3) In accordance with Article 34(2) of Regulation (EU) 2017/745, the Commission requested an independent audit on the Eudamed electronic systems for which the development has been completed. Such electronic systems are the electronic system on registration of economic operators (‘Actors’), the UDI database and the electronic system for registration of devices (‘UDI and devices’), the electronic system on notified bodies and certificates (‘Notified bodies and certificates’), and the electronic system on market surveillance (‘Market surveillance’).
(4) On the basis of the independent audit report of 18 June 2025 on the ‘Actors’, ‘UDI and devices’, ‘Notified bodies and certificates’, and ‘Market surveillance’ electronic systems, the Commission has verified that such electronic systems are functional and meet the relevant functional specifications drawn up pursuant to Article 34(1) of Regulation (EU) 2017/745.
(5) As set out in Article 123(3), points (d) to (ec), of Regulation (EU) 2017/745 and Article 113(3), points (f) to (fd) of Regulation (EU) 2017/746, the transition periods for the obligations and requirements that relate to any of the electronic systems referred to in those Regulations are to start as from the date of publication of this Decision on the notice as referred to in Article 34(3) of Regulation (EU) 2017/745, informing that the relevant electronic systems are functional and meet the functional specifications.
(6) In order to ensure legal certainty and a clear timeline for the mandatory use of the electronic systems declared functional, this Decision should enter into force on the day of its publication.