Regulation 3 Amendment of EU tertiary legislation

Commission Decision 2002/364/EC of 7th May 2002 on common technical specifications for in vitro-diagnostic medical devices^f1;

Commission Regulation (EU) No 207/2012 of 9th March 2012 on electronic instructions for use of medical devices^f2;

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^f3;

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^f4.