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Chapter III IDENTIFICATION AND TRACEABILITY OF DEVICES, REGISTRATION OF DEVICES AND OF ECONOMIC OPERATORS, SUMMARY OF SAFETY AND CLINICAL PERFORMANCE, EUROPEAN DATABASE ON MEDICAL DEVICESF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 25Identification within the supply chain
  2. 26Medical devices nomenclature
  3. 27Unique Device Identification system
  4. 28UDI database
  5. 29Registration of devices
  6. 30Electronic system for registration of economic operators
  7. 31Registration of manufacturers, authorised representatives and importers
  8. 32Summary of safety and clinical performance
  9. 33European database on medical devices
  10. 34Functionality of Eudamed

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))