Gentian’s cystatin C immunoassaywas launched in 2006. The assay is FDA510(k) cleared since 2008 and CE-marked. It is a Particle-Enhanced Turbidimetric Immunoassay (PETIA) for in vitro testing of cystatin C in human plasma and serum samples. The test has documented high inter-instrument accuracy on a wide range of clinical chemistry analysers.
Particle-Enhanced Turbidimetric Immunoassay
With avian antibodies for reduced interference
Can be applied on most automated platforms
FDA510 (k) cleared and CE-marked
If you and your colleagues would like to learn more about cystatin C and how you could incorporate this test into clinical workflows within your organisation, please contact us via email@example.com or the form below: