What are the requirements for UDI registration of systems and procedural kits?
According to Article 29 (2) of MDR (EU) 2017/745, before placing a system or procedural set on the market under Article [...]
ufficiomarketing2025-07-10T13:59:55+02:00FAQ, UDI in Medical Devices|
According to Article 29 (2) of MDR (EU) 2017/745, before placing a system or procedural set on the market under Article [...]
ufficiomarketing2025-07-11T12:18:51+02:00FAQ, UDI in Medical Devices|
In the UDI vector (the GS1-128 or DataMatrix barcode on the label of the medical device), the expiry date must be [...]

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