EUDAMED last updated this device on Jul 29, 2026
503201921
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 →- 04049059516748
- Reference / catalog number
- 503201921
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.
503201921 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 Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.