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Section 3 Market surveillanceF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 88Market surveillance activities
  2. 89Evaluation of devices suspected of presenting an unacceptable risk or other non-compliance
  3. 90Procedure for dealing with devices presenting an unacceptable risk to health and safety
  4. 91Procedure for evaluating national measures at Union level
  5. 92Other non-compliance
  6. 93Preventive health protection measures
  7. 94Good administrative practice
  8. 95Electronic system on market surveillance

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))