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3. 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(1);
(b)Commission Regulation (EU) No 207/2012 of 9th March 2012 on electronic instructions for use of medical devices(2);
(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(3);
(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(4).
EUDN 2002/364.
EUR 2012/207.
EUR 2012/722.
EUR 2013/920.
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