EUDAMED last updated this device on Apr 29, 2026
LYS-3
8431673HETF03T7On the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- Spinreact S.A.U.
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 →- 08431673720292
- Reference / catalog number
- 1705110
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.
LYS-3 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Spinreact S.A.U.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.