EUDAMED last updated this device on Jul 22, 2026
ST2 (eCLIA)
B-06978139078457On 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 →- 06978139078457
- Reference / catalog number
- ST2 (eCLIA)
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.