New educational guide for the use of the European Medical Device Nomenclature (EMDN)

Manufacturers operating under the Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) are required to utilise the European Medical Device Nomenclature (EMDN) for regulatory submissions, device registration in EUDAMED, and sampling. To support consistent and compliant application, MedTech Europe released a practical guide to the use of the European Medical Device Nomenclature which: Assists in the…