The UK Medical Devices Regulations 2002 (SI 2002 No 618, as amended) implement the Directives for active implantable medical devices, medical devices and in vitro diagnostic medical devices (IVDs) in the UK. These regulations continue to have effect in Great Britain.
The UK Medicines and Healthcare products Regulatory Agency (MHRA) have started the process to update the UK regulations and indicated that they will continue to recognize European CE marking until 30 June 2023.
