According to Article 26 of Regulation 745/2017 on medical devices and Article 23 of Regulation 746/2017 on in-vitro diagnostic medical device, the European Commission is required to make available a medical device nomenclature to support the functioning of the future EUDAMED (European Database on Medical Devices). We are pleased to inform you that The European Medical Device Coordination Group (MDCG) plans to use Italy’s CND codes as the basis for the Eudamed device database nomenclature.”
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