Binx IO CT/NG Assay rapid antigen influenza A virus

influenza A virus

CLIA Waived for Whole Blood – Finger Stick

Shallow nasal swab sample collection

The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food

Not FDA cleared for this use

Binx IO CT/NG Assay rapid antigen influenza A virusSingle use Cartridge for the qualitative detection of Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG)* Point of care (POC) molecular PCR testing for Chlamydia and Gonorrhea in both male and female patients* 30 minute time to result* Single visit test and treat* FDA cleared and CLIA waived* Fully automated* Integrates with EMR LIS* Clear detected not detected results* Accuracy: FEMALE Chlamydia: Sensitivity 96. 1%, Specificity 99. 1%,