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EC-Medical Device Coordination Group: Guidance on Classification of Medical Devices, Nomenclature (EMDN), and Supply Continuity Obligations
The European Union continues to strengthen its medical device regulatory framework through updated guidance on device classification, nomenclature (EMDN), and supply chain transparency. These updates aim to improve regulatory clarity, traceability, and patient safety, particularly under the MDR and IVDR frameworks. Key developments include the Update – MDCG 2021-24 Rev.1: Guidance on classification of medical devices (April 2026), alongside supporting guidance documents on EM
Sharan Murugan
14 hours ago3 min read