Q&A - Regulation (EU) 2024/1860 Article 10a MDR and IVDR

Year of pubication
2024
Editor
Commission européenne [European Commission]
Language(s)
English
Theme(s)
Mediacl devices
Number of pages
12
Type(s)
Guides
Document format
Pdf
File size
1.64 Mb

The information obligation in case of interruption or discontinution of supply of certain medical devices and in vitro diagnostic medical devices

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