EUDAMED last updated this device on Jul 22, 2026
ST2 (eCLIA)
B-06978139078433On the marketIVDD — General
- Applicable legislation
- —
- Organization name
- Shenzhen Lifotronic Technology 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 →- 06978139078433
- Reference / catalog number
- 0320514804
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.
ST2 (eCLIA) is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Shenzhen Lifotronic Technology Co., Ltd.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.