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qualitative test intended for use in point-of-care or clinical laboratory settings for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae DNA by polymerase chain reaction
The binx health io CT/NG test
designed to be performed in the clinic or decentralized laboratory while the patient waits
can enable immediate treatment of positive patients
removing the need for presumptive treatment
improving compliance
and reducing loss to follow-up
First ever FDA 510(k)
CLIA-Waived CT/NG molecular test for males and females
enabling same-visit diagnosis and treatment
Gives results comparable to a laboratory-based test for chlamydia and gonorrhea in about 30 minutes rather than days or weeks
The binx health io CT/NG Assay is intended for use with female vaginal swab specimens
collected either by a clinician or self-collected by a patient in a clinical setting
or male urine specimens
as an aid in the diagnosis of symptomatic or asymptomatic Chlamydia trachomatis and/or Neisseria gonorrhoeae infection
ASSAY, CT/NG BINX HEALTH IO SNGL-USE CRT (50/CS) D/S
