Binx IO CT/NG Assay rapid antigen Results are for the in
Description
Results are for the in vitro detection and differentiation ofSARS-CoV-2
influenza A virus
The INDICAID™ COVID-19 Antigen Quality Controls are external liquid quality controls
Certificate of Compliance
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%,
Exchange/Return Notes
- We offer a 30-day return/exchange service after receiving.
- Final sale items are not eligible for returns or exchanges.
- To process your return/exchange, please contact us at [email protected]
- Please click here for more details>>> Return & Exchange Policy
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