Commission Implementing Regulation (EU) 2023/2713 of 5 December 2023 designating European Union reference laboratories in the field of in vitro diagnostic medical devices Basic information CELEX number: 32023R2713Official Journal: L_202302713 Form: Regulation Procedure number: --Languages: bg cs da de el en et fi fr ga hr hu it lv lt mt nl pl pt ro sk sl es sv Dates Date of document: Date of publication: Date of effect: December 9, 2023 Entry into force - Date pub. +3 See Art 2.1 October 1, 2024 Application - Partial application See Art 2.2 And 2.3 Modified by Modifies Affected by case Legal basis EuroVoc Vocabulary Operation of the Institutions Testing Medical diagnosis Internal market - Principles Protection of health and safety Public health EU reference laboratory Medical device Sampling Medical devices Disease prevention Research body Disease surveillance