Schedule 5, Part 4, paragraph 30A(3)

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