EUDAMED last updated this device on Jul 29, 2026
501201919
404905922N8On the marketClass IIa
- Applicable legislation
- —
- Organization name
- CeramOptec 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 →- 04049059515802
- Reference / catalog number
- 501201919
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.
501201919 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by CeramOptec GmbH. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.