It is the role of the Notified Bodies to support medical device manufacturers in defining how to assign Basic UDI-DIs to groups of devices, not GS1.
A guidance by the European Commission on Basic UDI-DI and UDI-DI assignment examples is to be released in 2020. Please check regularly the upload of Medical Device Coordination Group guidance documents through this link:https://ec.europa.eu/growth/sectors/medical-devices/new-regulations/guidance_en.
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