Regulation 9 Amendment to regulation 2 (interpretation) in relation to Great Britain
In regulation 2(1)f1 after the definition of “Regulation (EU) 2017/746” insert—
““Regulation (EU) 2022/1107” means Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications for certain class D in vitro diagnostic medical devices in accordance with Regulation (EU) 2017/746 of the European Parliament and of the Councilf2;”.
Annotations
Footnotes
- f1
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Relevant amending instruments are S.I. 2013/2327, 2021/873 and 2023/627.
- f2
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OJ No. L 178, 05.07.2022, p.3.