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Division 4.5.3 Product verificationF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. Assessment of the technical documentation
  2. Type-examinations
  3. Verification by examination and testing of every product batch

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))