EUDAMED last updated this device on Aug 8, 2026
6902
89040456900TKOn the marketClass I
- Applicable legislation
- —
- Organization name
- Vitromed Healthcare
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 →- 00890404569025
- Reference / catalog number
- 6902
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.
6902 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Vitromed Healthcare. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.