EUDAMED last updated this device on Aug 25, 2026
Lumipulse pTau 217 Plasma Controls <2x2C, CE>
54144700375HOn the marketIVDR Class B
- Applicable legislation
- —
- Organization name
- Fujirebio Europe N.V.
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 →- 05414470815463
- Reference / catalog number
- 81546
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.
Lumipulse pTau 217 Plasma Controls <2x2C, CE> is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by Fujirebio Europe N.V.. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.