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Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance) (revoked)

EU Regulation 2017/2185 · Adopted 23 November 2017 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

Commission Implementing Regulation (EU) 2017/2185

of 23 November 2017

on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council

(Text with EEA relevance) (revoked)

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Annotations to the whole text

Textual amendments

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Regulation revoked (with saving) (31.12.2020) by S.I. 2002/618, reg. 4M (as inserted by The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/791), regs. 1(1), 3(7) (as amended by S.I. 2020/1478, regs. 1(3), Sch. 2 para. 2); 2020 c. 1, Sch. 5 para. 1(1))

Contents

  1. 1List of codes Repealed
  2. 2Application for designation Repealed
  3. 3Entry into force Repealed
  4. Signature
  5. Annex I: The list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 Repealed
  6. CODES REFLECTING THE DESIGN AND INTENDED PURPOSE OF THE DEVICE Repealed
  7. Active devices Repealed
  8. 1Active implantable devices Repealed
  9. 2Active non-implantable devices for imaging, monitoring and/or diagnosis Repealed
  10. 3Active non-implantable therapeutic devices and general active non-implantable devices Repealed
  11. Non-active devices Repealed
  12. 1Non-active implants and long term surgically invasive devices Repealed
  13. 2Non-active non-implantable devices Repealed
  14. HORIZONTAL CODES Repealed
  15. 1Devices with specific characteristics Repealed
  16. 2Devices for which specific technologies or processes are used Repealed
  17. Annex II: The list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of in vitro diagnostic medical devices under Regulation (EU) 2017/746 Repealed
  18. CODES REFLECTING THE DESIGN AND INTENDED PURPOSE OF THE DEVICE Repealed
  19. 1Devices intended to be used for blood grouping Repealed
  20. 2Devices intended to be used for tissue typing Repealed
  21. 3Devices intended to be used for markers of cancer and non-malignant tumours Repealed
  22. 4Devices intended to be used for human genetic testing Repealed
  23. 5Devices intended to be used to determine markers of infections/immune status Repealed
  24. 6Devices intended to be used for non-infectious pathologies, physiological markers, disorders/impairments (except human genetic testing), and therapeutic measures Repealed
  25. 7Devices which are controls without a quantitative or qualitative assigned value Repealed
  26. 8Class A devices in sterile condition Repealed
  27. HORIZONTAL CODES Repealed
  28. 1In vitro diagnostic devices with specific characteristics Repealed
  29. 2In vitro diagnostic devices for which specific technologies are used Repealed
  30. 3In vitro diagnostic devices which require specific knowledge in examination procedures for the purpose of product verification Repealed
  31. 4In vitro diagnostic devices which require specific knowledge in laboratory and clinical disciplines for the purpose of product verification Repealed

1List of codesF1

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2Application for designationF1

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3Entry into forceF1

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Signature

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1Active implantable devicesF1

2Active non-implantable devices for imaging, monitoring and/or diagnosisF1

3Active non-implantable therapeutic devices and general active non-implantable devicesF1

1Non-active implants and long term surgically invasive devicesF1

2Non-active non-implantable devicesF1

1Devices with specific characteristicsF1

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2Devices for which specific technologies or processes are usedF1

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1Devices intended to be used for blood groupingF1

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2Devices intended to be used for tissue typingF1

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3Devices intended to be used for markers of cancer and non-malignant tumoursF1

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4Devices intended to be used for human genetic testingF1

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5Devices intended to be used to determine markers of infections/immune statusF1

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6Devices intended to be used for non-infectious pathologies, physiological markers, disorders/impairments (except human genetic testing), and therapeutic measuresF1

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7Devices which are controls without a quantitative or qualitative assigned valueF1

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8Class A devices in sterile conditionF1

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1In vitro diagnostic devices with specific characteristicsF1

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2In vitro diagnostic devices for which specific technologies are usedF1

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3In vitro diagnostic devices which require specific knowledge in examination procedures for the purpose of product verificationF1

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4In vitro diagnostic devices which require specific knowledge in laboratory and clinical disciplines for the purpose of product verificationF1

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