EUDAMED last updated this device on Jun 29, 2026
C-U2
803383793IMINTRCA10015UOn the marketClass I
- Applicable legislation
- —
- Organization name
- CEFLA s.c.
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 →- 08033837930174
- Reference / catalog number
- 70220000; 76100400; 95510162; 95510161; 95510167
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.
C-U2 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by CEFLA s.c.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.