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Verséa Diagnostics

Binx io CT/NG Assay

Binx io CT/NG Assay

Single-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%,
Gonorrhea: Sensitivity 100%, Specificity 99.9%
MALE
Chlamydia: Sensitivity 92.5%, Specificity 99.3%,
Gonorrhea: Sensitivity 97.3%, Specificity 100%
* CPT codes: 87491 CT, 87591 NG or 87801 with or without QW [Infections agent, multiple organisms]
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