Mandatory use of EUDAMED requires manufacturers to understand the database structure, registration processes, and responsibilities under EU regulations. This webinar provides a clear overview of the compulsory modules, key deadlines, and the role of the Authorized Representative (NB). Using the EUDAMED playground, participants will see practical examples of Actor Registration (ACT) and UDI/Device modules (UDI/DEV), gaining hands-on guidance to ensure accurate and compliant submissions.