The Medical Devices (In Vitro Diagnostic Devices etc.) (Amendment) Regulations 2024
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Change 1
4 Amendment to the Consumer Rights Act 2015
In the Consumer Rights Act 2015, Schedule 5 (investigatory powers etc.) is amended as follows— (a) in paragraph 8, after the definition of “Regulation (EU) 2017/745 on medical devices” insert— “Regulation (EU) 2017/746 on in vitro diagnostic medical devices” means Regulation (EU) 2017/746 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; ; (b) in paragraph 19(7A)(a)— (i) at the end of sub-paragraph (iii), omit “or”; (ii) at the end of sub-paragraph (iv), omit “and” and insert— or (v) Regulation (EU) 2017/746 on in vitro diagnostic medical devices, and ; (c) in paragraph 30A(3)(b), after “Regulation (EU) 2017/745 on medical devices” insert “or Regulation (EU) 2017/746 on in vitro diagnostic medical devices”.
4 Amendment to the Consumer Rights Act 2015
In the Consumer Rights Act 2015, Schedule 5 (investigatory powers etc.) is amended as follows— (a) in paragraph 8, after the definition of “Regulation (EU) 2017/745 on medical devices” insert— “Regulation (EU) 2017/746 on in vitro diagnostic medical devices” means Regulation (EU) 2017/746 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; ; (b) in paragraph 19(7A)(a)— (i) at the end of sub-paragraph (iii), omit “or”; (ii) at the end of sub-paragraph (iv), omit “and” and insert— or (v) Regulation (EU) 2017/746 on in vitro diagnostic medical devices, and ; (c) in paragraph 30A(3)(b), after “Regulation (EU) 2017/745 on medical devices” insert “or Regulation (EU) 2017/746 on in vitro diagnostic medical devices”.
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