EUDAMED last updated this device on Jun 3, 2026
CLAVIVIT 380
42500483SchultArm9XOn the marketClass I
- Applicable legislation
- —
- Organization name
- Orpedo GmbH
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 →- 04000001031207
- Reference / catalog number
- 208-380
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.
CLAVIVIT 380 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Orpedo GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.