We support you with EUDAMED registration of your devices

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!