EUDAMED last updated this device on May 23, 2026
INSTRUMENT CASE UNIVERSAL SCREWDRIVER SET
++D800INSTRUMCASE01SQ- 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 →- D800SIAK60010
- Reference / catalog number
- SIAK6001
INSTRUMENT CASE UNIVERSAL SCREWDRIVER SET 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 Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.