OverviewEUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746…Actors registrationThe Actor registration is the first of the six EUDAMED modules.Înregistrarea identificatorului unic al dispozitivului (UDI)Regulamentul (UE) 2017/745 privind dispozitivele medicale și Regulamentul (UE) 2017/746 privind dispozitivele medicale pentru diagnostic in vitro introduc un identificator unic ...Notified Bodies and CertificatesRegulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) establish that Notified… Latest updatesNews announcement14 martie 2023The new UDI Helpdesk is live. It helps the economic operators to implement the requirements introduced by the unique device identification system1 min de lecturăNews announcement16 decembrie 2022Functional specifications for the European Database on Medical Devices (EUDAMED)1 min de lecturăNews announcement2 august 2022Version 2.8 of Technical documentation - UDI/Devices registration1 min de lecturăNews announcement11 aprilie 2022The EUDAMED UDI/Devices module updated technical documentation is available1 min de lecturăVedeți tot HighlightsThe EUDAMED Information Centre is the central point of support for EUDAMED users, presenting action steps and process logic from a wide range of documentationThe UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI systemFactsheet on MDR requirements for Transparency and Public Information DocumentsPublications
OverviewEUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746…
Înregistrarea identificatorului unic al dispozitivului (UDI)Regulamentul (UE) 2017/745 privind dispozitivele medicale și Regulamentul (UE) 2017/746 privind dispozitivele medicale pentru diagnostic in vitro introduc un identificator unic ...
Notified Bodies and CertificatesRegulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) establish that Notified…
News announcement14 martie 2023The new UDI Helpdesk is live. It helps the economic operators to implement the requirements introduced by the unique device identification system1 min de lectură
News announcement16 decembrie 2022Functional specifications for the European Database on Medical Devices (EUDAMED)1 min de lectură
News announcement2 august 2022Version 2.8 of Technical documentation - UDI/Devices registration1 min de lectură
News announcement11 aprilie 2022The EUDAMED UDI/Devices module updated technical documentation is available1 min de lectură
The EUDAMED Information Centre is the central point of support for EUDAMED users, presenting action steps and process logic from a wide range of documentation
The UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI system
