The European Medical Device Nomenclature (EMDN), as established by Article 26 of Regulation (EU) 2017/745 and Article 23 of Regulation (EU) 2017/746, will be updated annually based on real world and user feedback. stakeholders.
The document MDCG 2024-2 Procedures for the updates of the European Medical Device Nomenclature defines the procedure for the annual review of the EMDN and for so-called ad hoc requests. In particular, the document:
identifies the actors involved in the management and updating process of the EMDN (the Nomenclature-WG, the EMDN-TT technical group, the stakeholders) establishes the Phases through which each actor intervenes, with different tasks and objectives, in updating the EMDN .
Requests from stakeholders are collected through the Submission platform for EMDN proposals.
For further information, consult the page: The EMDN update