EUDAMED last updated this device on Jul 5, 2026
VeriPlate
763003261010438223On the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- Hamilton AG
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 07630032600256
- Reference / catalog number
- 10104382
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
VeriPlate is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Hamilton AG. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.