EUDAMED registration support

The deadline for EUDAMED registration is approaching. By 28th of November, all medical devices and IVDs placed on the market must be registered in the EUDAMED database – regardless of whether they are certified under the MDR/IVDR or as legacy devices under the MDD/IVDD.

Manually entering more than 100 data fields per UDI-DI represents a significant effort, especially for manufacturers with large product portfolios.

With our XML Bulk Upload process, we support you in registering your product portfolio in EUDAMED quickly and cost‑efficiently.

•     Structured capture of all required product data
•     Significant reduction of manual data entry
•     Scalable approach for large portfolios
•     Transparent and traceable data preparation for XML upload
•     Lower error potential through standardized templates

Bonus: The prepared dataset can also be used for the swissdamed bulk upload.

If you need assistance with registering your device portfolio, feel free to contact us!