EUDAMED Actor Registration Module
11 May 2023UK Registration Deadline: High-Risk Devices
11 May 2023The UK is no longer recognized as part of the EU.
Manufacturers in Great Britain (England, Scotland, Wales) require an EU Authorized Representative to continue marketing in the EU, and EU manufacturers must appoint a UK Responsible Person and register their devices with the UK MHRA.
The MHRA provides a one-year transition period to register devices, exact dates depend on the device classification. The EU does not provide a transition period.