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Schedule 5, Part 4, paragraph 30A

CRA 2015
Consumer Rights Act 2015 · United Kingdom

The power in sub-paragraph (2) is available to an officer of a domestic enforcer acting pursuant to— the duty in regulation 61(1A) or (1B) of the Medical Devices Regulations 2002 (S.I. 2002/618), a duty in regulations made under section 15(1) of the Medicines and Medical Devices Act 2021, or the duty in regulation 26 of the Medical Devices (Northern Ireland Protocol) Regulations 2021. The officer may decommission or switch off any relevant medical device which is installed at a given location. In sub-paragraph (2), “relevant medical device” means— where a domestic enforcer is acting pursuant to a duty mentioned in sub-paragraph (1)(a) or (b), any medical device to which the Medical Devices Regulations 2002 apply; where a domestic enforcer is acting pursuant to the duty mentioned in sub-paragraph (1)(c), any medical device to which Regulation (EU) 2017/745 on medical devices or Regulation (EU) 2017/746 on in vitro diagnostic medical devices applies.

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Source: legislation.gov.uk · retrieved 2026-07-30