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Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications for certain class D in vitro diagnostic medical devices in accordance with Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance)
C/2022/4498
In force
- CELEX number:
- 32022R1107
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 04/07/2022; Date of adoption
- Number of pages:
- 54
Commission Implementing Regulation (EU) 2022/944 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the tasks of and criteria for European Union reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)
C/2022/4311
In force
- CELEX number:
- 32022R0944
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 17/06/2022; Date of adoption
- Number of pages:
- 13
Commission Implementing Regulation (EU) 2025/2526 of 16 December 2025 amending Implementing Regulation (EU) 2023/2713 to correct the designation of an EU reference laboratory and to designate European Union reference laboratories for in vitro diagnostic medical devices intended for detection or quantification of markers of parasite infection and detection of blood grouping markers
C/2025/8634
In force
- CELEX number:
- 32025R2526
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 16/12/2025; Date of adoption
Commission Implementing Regulation (EU) 2023/2713 of 5 December 2023 designating European Union reference laboratories in the field of in vitro diagnostic medical devices
C/2023/8234
In force
- CELEX number:
- 32023R2713
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 05/12/2023; Date of adoption
Commission Implementing Regulation (EU) 2022/945 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and the Council with regard to fees that may be levied by EU reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)
C/2022/4047
In force
- CELEX number:
- 32022R0945
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 17/06/2022; Date of adoption
- Number of pages:
- 3
Commission Implementing Decision (EU) 2019/939 of 6 June 2019 designating issuing entities designated to operate a system for the assignment of Unique Device Identifiers (UDIs) in the field of medical devices (Text with EEA relevance.)
C/2019/4068
In force
- CELEX number:
- 32019D0939
- Form:
- Implementing decision
- Author:
- European Commission, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
- Date of document:
- 06/06/2019; Date of adoption
- Number of pages:
- 3
Commission Implementing Decision (EU) 2024/2120 of 30 July 2024 renewing the designation of issuing entities designated to operate a system for the assignment of Unique Device Identifiers (UDIs) in the field of medical devices
C/2024/5541
In force
- CELEX number:
- 32024D2120
- Form:
- Implementing decision
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 30/07/2024; Date of adoption
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. )
C/2017/7779
In force
- CELEX number:
- 32017R2185
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
- Date of document:
- 23/11/2017; Date of adoption
- Number of pages:
- 11
Commission Implementing Regulation (EU) 2026/977 of 4 May 2026 laying down certain uniform quality management and procedural requirements for the conformity assessment activities carried out by a notified body designated under Regulations (EU) 2017/745 and (EU) 2017/746 of the European Parliament and of the Council
C/2026/2798
In force
- CELEX number:
- 32026R0977
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 04/05/2026; Date of adoption
Domain: All, Subdomain: Legal acts, Implementing acts: CELEX number: 32017R0746, Search language: English