Medical professionals around the world use BinaxNOW® rapid in vitro diagnostic tests to identify a variety of infectious diseases at the point of care. Our technologies detect bacteria and viruses causing upper and lower respiratory tract infections, including Legionnaires' disease, pneumonia, RSV and influenza, as well as pathogens causing filariasis and malaria.
Rapid and accurate test results provide the foundation for pathogen-specific diagnosis, facilitating optimal patient management and infection control practices.
BinaxNOW® Legionella Urinary Antigen Test is a rapid assay for the qualitative detection of Legionella pneumophila serogroup 1 antigen in urine samples from patients with symptoms of pneumonia.
BinaxNOW® S. pneumoniae is a rapid assay for the qualitative detection of S. pneumoniae antigen in the urine of patients with pneumonia and in the cerebral spinal fluid (CSF) of patients with meningitis.
BinaxNOW® Influenza A & B is an in vitro immunochromatographic assay for the qualitative detection of influenza A and B nucleoprotein antigens in nasopharyngeal (NP) swab, nasal swab samples and nasal wash/aspirate specimens.
BinaxNOW® RSV is an in vitro rapid immunochromatographic assay used to detect respiratory syncytial virus (RSV) fusion protein antigen in nasal wash and nasopharyngeal (NP) swab specimens from symptomatic patients.
The BinaxNOW® G6PD Test is a visual screening test used for differentiating normal from deficient G6PD activity levels in whole blood and is intended to aid in the identification of people with G6PD deficiency.
The BinaxNOW® Strep A Test is a rapid immunochromatographic assay for the qualitative detection of Streptococcus pyogenes Group A antigen from throat swab specimens to aid in the diagnosis of Group A pharyngitis.
The BinaxNOW® S. aureus test is a rapid qualitative immunochromatographic assay that provides a presumptive identification of S. aureus direct from blood culture that has Gram-positive cocci in clusters (GPCC).
The BinaxNOW® Malaria test is an in vitro immunochromatographic assay for the qualitative detection of Plasmodium antigens circulating in human venous and capillary EDTA whole blood of individuals with signs and symptoms of malarial infection.
The BinaxNOW® Malaria Positive Control is intended for use as an assayed positive external quality control with the qualitative BinaxNOW® Malaria Test. It is designed for routine use to aid in verifying proper performance of the procedure and the antigen detection reagents of the BinaxNOW® Malaria Test.
Binax™ Legionella Urinary Antigen EIA kit is an enzyme immunoassay (EIA) based system intended to qualitatively detect the presence of Legionella pneumophila serogroup 1 antigen in urine as an adjunct to culture for the presumptive diagnosis of past or current Legionnaires’ disease.