Regulation 5 Amendments to regulation 2 (interpretation)
In regulation 2(1)f1 after the definition of “Regulation (EU) No 722/2012” insert—
““Regulation (EU) 2017/745” means Regulation (EU) 2017/745f2 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC;
“Regulation (EU) 2017/746” means Regulation (EU) 2017/746f3 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU;”.
Annotations
Footnotes
- f1
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Relevant amending instruments are S.I. 2013/2327, 2021/873.
- f2
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OJ No. L 117, 5.5.2017, p.1; amended by OJ No. L130, 24.4.2020, p.18 and OJ No. L80, 20.03.2023, p.24.
- f3
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OJ No. L 117, 5.5.2017, p.176; amended by OJ No. L19, 28.1.2022, p.3 and OJ No. L80, 20.03.2023, p.24.