EUDAMED last updated this device on Aug 31, 2026
VE105RS
697377067307NVOn the marketClass IIb
- Applicable legislation
- —
- Organization name
- Comepa medical device Co., Ltd
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 →- 06973770670060
- Reference / catalog number
- VE105RS
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.
VE105RS is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Comepa medical device Co., Ltd. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.