Binx IO CT/NG Assay rapid antigen Results are for the in

Results are for the in vitro detection and differentiation ofSARS-CoV-2

20 disposable plastic fixed volume pipettes (for whole blood only) packed in one pvc re-sealable bag

influenza A virus

Not FDA cleared for this use

Binx IO CT/NG Assay rapid antigen Results are for the inSingle 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%,