Regulation 10 Amendment to regulation 2 (interpretation) in relation to Northern Ireland

In regulation 2(1)^f1 after the definition of “Regulation (EU) 2017/745” insert—

• ““Regulation (EU) 2017/746” means Regulation (EU) 2017/746^f2 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;

• “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 Council^f3;”.