EUDAMED last updated this device on Aug 13, 2026
SCREWDRIVER HANDPIECE
++D800SCREWDHANDP0157On the marketClass I
- Applicable legislation
- —
- Organization name
- Zirkonzahn SRL
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 →- D800SIAK11010
- Reference / catalog number
- SIAK1101
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.
SCREWDRIVER HANDPIECE is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Zirkonzahn SRL. Placed on the EU market in Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.