# The Medical Devices (In Vitro Diagnostic Devices etc.) (Amendment) Regulations 2023, Regulation 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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Source: https://www.legislation.gov.uk/ukdsi/2023/9780348253696/regulation/4 (the official version)
Page: https://openlegislation.uk/draft-medical-devices-in-vitro-diagnostic-devices-etc-amendment-regulations-2023/regulation-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.