Choose the experimental features you want to try

This document is an excerpt from the EUR-Lex website

Search Results

Sort by

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

Legal status of the documentIn 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

Legal status of the documentIn 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) 2022/1107 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

Legal status of the documentIn 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

Legal status of the documentIn 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) 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

Legal status of the documentIn 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 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

Legal status of the documentIn 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
Sort by
Domain: All, Form: Implementing regulation, Implementing acts: CELEX number: 32017R0746, Search language: German