Document:EU MDCG Guidelines -

Document information
Reference	EU MDCG Guidelines -
Validity area	EU
Scope(s)	MD
Document name	MDCG Guidelines
Version / Revision	-
Status	N.A.
Document type	Corpus of texts
Language(s)	EN
Description	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
Official source	Official link
Restricted access	No
Submitted by	Florian Adragna
Contributors