EUDAMED last updated this device on Aug 25, 2026
DIO Straight Drill
880004924022AZOn the marketClass IIa
- Applicable legislation
- —
- Organization name
- DIO Corporation
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 →- 08800049403372
- Reference / catalog number
- DSU 2713S11
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.
DIO Straight Drill is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by DIO Corporation. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.