Binx io

Binx io is the first ever, FDA-cleared, molecular point-of-care platform that enables clinicians to test and treat women and men for the most common STIs, chlamydia and gonorrhea, in a single office visit.
Binx io is a small, desktop instrument that processes a single-use, assay-specific cartridge with no sample preparation necessary. (Request a Quote to inquire about the analyzer and cartridges/tests)
The Binx io has been cleared by the FDA for use in point-of-care and clinical laboratory settings for the rapid and accurate detection of chlamydia and gonorrhea in vaginal swab and first catch urine samples collected by either a clinician or patient.
Uses ultra-rapid polymerase chain reaction (PCR) amplification in conjunction with our proprietary electrochemical detection to achieve sensitivity and specificity on par with central lab performance.

A CLIA number is required for purchase. Your order will NOT ship without providing it.

DPP HIV-Syphilis

binx io

Features

FDA-Cleared, CLIA-Waived
Detects Chlamydia and Gonorrhea in both men and women
30 minute turnaround time
Vaginal Swabs or First Catch Urine Samples

Packaging

Test System Components:
The binx io Instrument for running the Cartridge;
The binx io CT/NG Cartridge (or “Cartridge”), which contains all the necessary reagents to perform the binx io CT/NG Assay on the binx io Instrument;
A single-use, fixed-volume transfer pipet (packaged with the Cartridge) for transferring the sample to the Cartridge;
The Vaginal Swab Specimen Collection Kit;
The Male Urine Collection Kit.

Resources

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