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and preservation of DNA in a male urine sample for use with the binx io CT/NG Assay
The INDICAID™ COVID-19 Antigen Quality Controls are external liquid quality controls
influenza A virus
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
Binx IO CT/NG Assay rapid antigen and preservation of DNA 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%,
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