Eudamed

The new regulations on medical devices (MDR) and on in vitro diagnostic medical devices (IVDR) establish a much wider EUDAMED database than the existing

EUDAMED will help to ensure that patients continue to receive good quality health care, and a high level of health protection, making sure that incompatible

MDR Eudamed services, technical and non technical training, support, UDI data uploads / downloads. eDelivery Access point. UDI, Clinical investigations, and

Oct 30, 2019 - The European Commission recently concluded that its database of medical device information (Eudamed) will only be operational once all

Jan 22, 2018 - European regulators are on track for launching the Eudamed database for medical devices in early 2020. Learn more about European medical

Aug 5, 2018 - Compliance with Eudamed database requirements under the European Medical Devices Regulation (MDR) and In-vitro Diagnostics

EUDAMED, the European Databank for Medical Devices, attends to the administration of medical devices. The Medical Device Regulation relies on Eudamed,

Eudamed is the European Databank on Medical Devices. It's a secure, web-based portal that acts as a central hive for the exchange of information between