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Annex XI CONFORMITY ASSESSMENT BASED ON PRODUCTION QUALITY ASSURANCEF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 1Division 1
  2. 2Division 2
  3. 3Quality management system
  4. 4Surveillance
  5. 5Verification of manufactured class D devices
  6. 6Administrative provisions

Annotations

Textual amendments

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))