EUDAMED last updated this device on Jun 8, 2026
VYTIL
697261114AUXCONNECTORMDOn the marketClass I
- Applicable legislation
- —
- Organization name
- SUZHOU GZM MEDICAL 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 →- 06972611142773
- Reference / catalog number
- VTL/CN05
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.
VYTIL is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SUZHOU GZM MEDICAL CO., LTD. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.