EUDAMED last updated this device on Sep 7, 2026
230241FX
B-04250407785246On the marketClass I
- Applicable legislation
- —
- Organization name
- FENTEX medical 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 →- 04250407785246
- Reference / catalog number
- 230241FX
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.
230241FX is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by FENTEX medical GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.