]> 2026-10-07T14:17:59+02:00 Document:EU MDCG Guidelines - 3000 en EMA – Medical Device Coordination Group (MDCG) Guidance - MDCG endorsed documents and other guidance: - Annex XVI products (Regulation EU 2017/745) - Borderline and Classification - Class I Devices - Clinical investigation and evaluation - COVID-19 - Custom-Made Devices - European database on medical devices (EUDAMED) - European Medical Device Nomenclature (EMDN) - Implant cards - In-house devices - Authorised Representatives, Importers, Distributors - In Vitro Diagnostic medical devices (IVD) - New technologies - Notified bodies - Person responsible for regulatory compliance (PRRC) - Post-Market Surveillance and Vigilance (PMSV) - Standards - Unique Device Identifier (UDI) - Other topics - Other guidance documents EN MDCG Guidelines EU MDCG Guidelines - No MD N.A. Florian Adragna Corpus of texts EU - 2026-07-16T10:54:48Z 2461237.9547222 EU MDCG Guidelines - 3000 1 table 3 [[Reference:+]] [[HasDocument::Document:EU MDCG Guidelines -]] EU MDCG Guidelines -# QUERY1433a03b0333d8ed422a207178bd7020