Lumipulse® G pTau 217 Plasma (CE marked (IVDR))

Lumipulse G pTau 217 Plasma is a test for in vitro diagnostic use with the automated LUMIPULSE G System for the quantitative measurement of Tau phosphorylated at threonine 217 (pTau 217) in human plasma (K2EDTA).

The Lumipulse G pTau 217 Plasma assay is intended to aid Healthcare providers to identify patients with amyloid pathology associated with Alzheimer’s disease.

The test is indicated for patients, aged 50 years and over, presenting with signs and symptoms of cognitive decline in a specialized care setting. The Lumipulse G pTau 217 Plasma assay is to be used as an adjunct to other diagnostic evaluations. This product is for professional use only.

CE marked (IVDR)

Please contact your local Fujirebio representative for the availability of this product in your country.