EUDAMED registration is now an important part of regulatory compliance for medical device and IVD companies operating on the EU market.
As of 28 May 2026, mandatory use of key EUDAMED modules has started, including Actor Registration and UDI/Device Registration.
Aurevia can support your organization throughout the EUDAMED registration process, including:
• Actor registration and SRN support
• UDI and device registration
• Basic UDI-DI and UDI-DI registration support
• EMDN code identification
• Review and preparation of required registration information
• Support for legacy device registration
• Guidance on MDR and IVDR registration requirements
• Practical support throughout the EUDAMED registration process
Whether you are registering for the first time, preparing device data or need support reviewing existing registrations, our QA/RA consultants can help you navigate the requirements and ensure that the required information is complete and consistent.
Need help with EUDAMED? Contact us to discuss how we can support your registration activities.