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Section 2 Conformity assessmentF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 52Conformity assessment procedures
  2. 53Involvement of notified bodies in conformity assessment procedures
  3. 54Clinical evaluation consultation procedure for certain class III and class IIb devices
  4. 55Mechanism for scrutiny of conformity assessments of certain class III and class IIb devices
  5. 56Certificates of conformity
  6. 57Electronic system on notified bodies and on certificates of conformity
  7. 58Voluntary change of notified body
  8. 59Derogation from the conformity assessment procedures
  9. 60Certificate of free sale

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))