A number of different topics are relevant for the implementation of the Medical Devices Regulations: the number of areas is vast and includes, among others:
- Notified bodies
- Unique Device Identifier (UDI)
- Reprocessing
- Harmonised standards
- Combined studies
- Counterfeiting
- Custom-made devices
- The European medical devices nomenclature (EMDN)
- In-house medical devices
- Software and apps
For further information on Topics of Interest
