| 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.