|Theme||European MD nomenclature (EMDN)|
|Target audience||All actors|
|Products concerned||MD, IVD|
|Regulatory references||MDR (EU) 2017/745
IVDR (EU) 2017/746
The purpose of this guide is to clarify the criteria and requirements for the future European medical devices nomenclature.
Note: Since the publication of this guide, the Italian CND nomenclature has been designated.