Page summary:
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Change made:
Changes to registration requirements for Northern Ireland effective 28 May 2026Updated Fees implementation guidance; clarification concerning fee waivers and new section for Northern Ireland feesIVDs undergoing performance evaluation; minor updates to textCoronavirus test device approval (CTDA) and registering with MHRA; minor updates to textChanges to Public register of manufacturers section; medical device brand/trade name will be displayed on PARD from 23 February 2026, and further information concerning use of GMDN®
