The role of EUDAMED



What is EUDAMED?

EUDAMED is the IT system developed by the European Commission to implement MDR Regulation (EU) 2017/745 on medical devices and IVDR Regulation (EU) 2017/746  on in vitro diagnostic medical devices.

EUDAMED will improve transparency and coordination of information regarding medical devices available on the EU market. The system will be multipurpose. It will function as a registration system, a collaborative system, a notification system, and a dissemination system (open to the public) and will be interoperable.

  • Actors registration
  • UDI / Devices registration
  • Notified Bodies and Certificates
  • Clinical Investigations and performance studies
  • Vigilance and post-market surveillance
  • Market Surveillance

The module on Actor registration will be the first module made available. The deployment of the module is planned for December 2020. The first module will be on the Economic Operator (EO) registration and will be on a voluntary basis. The EO’s are manufacturers, system/procedure pack producers, authorized representatives, and importers.

It is important to start the registration of EO as soon as the system is available (currently planned for December 2020), for the reason that the EO’s need an SRN (Single Registration Number). Only if you have an SRN it will be possible to utilize other EUDAMED modules and to apply for conformity assessment. The advantage to undertake voluntary EO registration now is that manufacturers can wait without time pressure on the validation of the registration by the competent authority (CA). The EUDAMED modules on device& UDI registration and on certificates & notified bodies are planned to be launched by May 2021.


EUDAMED Training

Learn more about EUDAMED. Qserve will provide several training courses on EUDAMED. The first one will be to educate manufacturers on the process, timelines, and the impact of the Eudamed system.

Learning Objectives:

  • Introduction to EUDAMED
  • EUDAMED readiness and timelines
  • Data needed in the EO registration module for all actors
  • Data needed in the device & UDI registration module
  • Practical guidance on operating EUDAMED, including outsourcing registrations

More information about the EUDAMED Training



Interested in our EUDAMED service?

We would like to tell you more about the possibilities that Qserve offers as a Regulatory Consultant.

Information Request