These Regulations amend the Medical Devices Regulations 2002 (S.I. 2002/618) (the 2002 Regulations) by removing the 25th and 26th May 2025 revocation dates of the following pieces of assimilated EU law; – Commission Decision 2002/364 (on common technical specifications for in vitro medical devices), – Commission Regulation (EU) No 207/2012 (on electronic instructions for use of medical devices), – Regulation (EU) No 722/2012 (concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin) and – Regulation (EU) No 920/2013 (on the designation and the supervision of notified bodies under Council Directive 90/385/EEC on active implantable medical devices and Council Directive 93/42/EEC on medical devices).
UK – The Medical Devices (Amendment) (Great Britain) Regulations 2025
