UDI database
Article 25
The Commission, after consulting the MDCG, shall set up and manage a UDI database in accordance with the conditions and detailed arrangements provided for in Article 28 of Regulation (EU) 2017/745.
Regulation (EU) 2017/746 Article 25
Regulation (EU) 2017/746 Article 25
Other provisions in CHAPTER III — IDENTIFICATION AND TRACEABILITY OF DEVICES, REGISTRATION OF DEVICES AND OF ECONOMIC OPERATORS, SUMMARY OF SAFETY AND CLINICAL PERFORMANCE, EUROPEAN DATABASE ON MEDICAL DEVICES
- Article 22: Identification within the supply chain
- Article 23: Medical devices nomenclature
- Article 24: Unique Device Identification system
- Article 26: Registration of devices
- Article 27: Electronic system for registration of economic operators
- Article 28: Registration of manufacturers, authorised representatives and importers
- Article 29: Summary of safety and performance
- Article 30: European database on medical devices
CitationArticle 25 of Regulation (EU) 2017/746 (LawPlayer, data as of 2026-07-04)
© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.
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