CHAPTER VII U.K. POST-MARKET SURVEILLANCE, VIGILANCE AND MARKET SURVEILLANCE

Section 3 U.K. Market surveillance

F1 Article 90 U.K. Procedure for dealing with devices presenting an unacceptable risk to health and safety

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Textual Amendments applied to the whole legislation

F1 Regulation revoked (31.12.2020) by The Medical Devices Regulations 2002 (S.I. 2002/618), reg. 4P (as inserted by S.I. 2019/791, regs. 1(1), 3(7) (as amended by S.I. 2020/1478, regs. 1(3), Sch. 2 paras. 2, 9(m)); 2020 c. 1, Sch. 5 para. 1(1))