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Division 22 Protection against the risks posed by medical devices intended by the manufacturer for use by lay personsF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 22.1Division 22.1
  2. 22.2Division 22.2
  3. 22.3Division 22.3

Annotations

Textual amendments

F1

Regulation revoked (31.12.2020) by The Medical Devices Regulations 2002 (S.I. 2002/618), reg. 4O (with savings and transitional provisions for N.I. in reg. 3ZA) (as amended by S.I. 2019/791, regs. 1(1), 3(7) and by S.I. 2020/1478, regs. 1(3), Sch. 2 para. 2; and as amended (27.7.2021) by The Medical Devices (Northern Ireland Protocol) Regulations 2021 (S.I. 2021/905), regs. 1(2), 4, 32); 2020 c. 1, Sch. 5 para. 1(1))