Theme European MD nomenclature (EMDN)
Target audience All actors
Products concerned MD, IVD
Regulatory references MDR (EU) 2017/745

Article 26

IVDR (EU) 2017/746

Article 23

Documents mentioned


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.