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Chapter II MAKING AVAILABLE ON THE MARKET AND PUTTING INTO SERVICE OF DEVICES, OBLIGATIONS OF ECONOMIC OPERATORS, REPROCESSING, CE MARKING, FREE MOVEMENTF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 5Placing on the market and putting into service
  2. 6Distance sales
  3. 7Claims
  4. 8Use of harmonised standards
  5. 9Common specifications
  6. 10General obligations of manufacturers
  7. 11Authorised representative
  8. 12Change of authorised representative
  9. 13General obligations of importers
  10. 14General obligations of distributors
  11. 15Person responsible for regulatory compliance
  12. 16Cases in which obligations of manufacturers apply to importers, distributors or other persons
  13. 17Single-use devices and their reprocessing
  14. 18Implant card and information to be supplied to the patient with an implanted device
  15. 19EU declaration of conformity
  16. 20CE marking of conformity
  17. 21Devices for special purposes
  18. 22Systems and procedure packs
  19. 23Parts and components
  20. 24Free movement

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))