EUDAMED last updated this device on Jul 17, 2026
SCAN-DM10
84356503ScanbodiesR9On the marketClass I
- Applicable legislation
- —
- Organization name
- BIONER SA
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 →- 08435650311084
- Reference / catalog number
- SCAN-DM10
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.
SCAN-DM10 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by BIONER SA. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.