EUDAMED last updated this device on Feb 3, 2026
VIDAS® T3
357302BUDI000087TGOn the marketIVDR Class B
- Applicable legislation
- —
- Organization name
- bioMérieux SA
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 →- 03573026064891
- Reference / catalog number
- 30403
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.
VIDAS® T3 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by bioMérieux SA. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.