EU: MDCG publishes requirements for medical device nomenclature

Standardised, freely accessible nomenclature for medical devices is being introduced as part of the implementation of the new EU regulation on medical devices (2017/745) and in-vitro diagnostics (2017/756). The Medical Device Coordination Group (MDCG) has now published a requirements profile for this nomenclature, which can be downloaded from the EU website.

https://ec.europa.eu/docsroom/documents/28668

 

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