Register medical devices to place on the market
Register medical devices to place on the market How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland From: Contents MHRA under existing arrangements: MHRA subject to grace periods, depending on the class of devices. In Great Britain devices must conform to the Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002) as they apply in Great Britain so that they ...
United Kingdom Northern Ireland Great Britain Medical Devices Regulations United Kingdom Responsible Persons Authorised Representatives
Source: gov.uk