EUDAMED last updated this device on Jul 7, 2026
VE3019
B-FRMF000009778VE3019Q7On the marketClass IIb
- Applicable legislation
- —
- Organization name
- CAHOUET
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 →- D-FRMF000009778VE3019Q7
- Reference / catalog number
- VE3019
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.
VE3019 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by CAHOUET. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.