# The Medical Devices (Amendment) (EU Exit) Regulations 2021, Regulation 3: Amendment of EU tertiary legislation


The following EU tertiary legislation concerning medical devices is amended in accordance with Schedule 2—
(a) Commission Decision 2002/364/EC of 7th May 2002 on common technical specifications for in vitro-diagnostic medical devices;
(b) Commission Regulation (EU) No 207/2012 of 9th March 2012 on electronic instructions for use of medical devices;
(c) Commission Regulation (EU) No 722/2012 of 8th August 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;
(d) Commission Implementing Regulation (EU) No 920/2013 of 24th September 2013 on the designation and supervision of notified bodies under Council Directive 90/385/EEC on active implantable medical devices and Council Directive 93/42 on medical devices.

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Source: https://www.legislation.gov.uk/uksi/2021/873/regulation/3 (the official version)
Page: https://openlegislation.uk/medical-devices-amendment-eu-exit-regulations-2021/regulation-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.