Binaxnow Streptococcus Pneumoniae

Abbott BinaxNOW S. pneumoniae Antigen Card provides accurate, rapid identification of S. pneumoniae antigen in patients with pneumococcal pneumonia and pneumococcal meningitis with an easy-to-use technology, aiding physicians in providing rapid, focused therapy. Time to Result: 15 minutes Performance data: Urine Sensitivity/Specificity 86% / 94% CSF Sensitivity/Specificity 97% / 99% Ordering Information Cat No. Description Specimen Pack size 710000 Streptococcus Urine, CSF 22 Tests Pneumoniae Ag card

PERFORMANCE SPECIFICATIONS 1. Detection limitation: 200 copies /mL. 2. Precision: using precision reference CV1 and CV2 for within-batch and between-batch detection, the coefficient of variation (CV) of their Ct values is â?¤ 5.0%. 3. Conformity rate of Negative Control: 100% 4. Conformity rate of Positive Control: 100% 5. Specificity: This product will not cross react with positive samples of human coronavirus HKU1 OC43, NL63 and 229E, SARS coronavirus, MERS corona-virus, H1N1 (new influenza A (H1N1) virus (2009), the seasonal H1N1) and H3N2, H5N1, H7N9, influenza B Yamagata, Victoria, respiratory syncytial virus type A, B, parainfluenza type 1, 2, 3, rhinovirus species A, B and C, adenovirus, 1, 2, 3, 4, 5, 7 and 55, enterovirus species A, B, C, D,Human pulmonary virus, partial pulmonary virus, EB virus, measles virus, human cytomegalo virus, rotavirus, norovirus, mumps virus, varicella-zoster virus and mycoplasma pneumoniae, chlamydia pneumoniae, legionella, bordetella pertussis, haemophilus influenzae, staphylococcus aureus, streptococcus pneumoniae, pyogenic streptococcus, klebsiella pneumoniae, mycobacterium tuberculosis, pyogenic streptococcus, candida albicans, candida glabrata, newborn Cryptococcus and human genome DNA.

Product Details: Number of Reactions(Preps)/Kit 22T Brand Abbott Result Time (Rapid Kits) 15 Min Cat. No 852-000 BinaxNOW Legionella Urinary Antigen Card is a rapid assay for the qualitative detection of Legionella pneumophila serogroup 1 antigen in urine samples from patients with symptoms of pneumonia. It is intended to aid in the presumptive diagnosis of Legionnaires disease caused by L. pneumophila serogroup 1 in conjunction with culture and other methods. Sample Type: Urine Time to Result: 15 minutes Kit Size: 22 tests Performance Data: Sensitivity/Specificity: 95%/95%

Product Details: Number of Reactions(Preps)/Kit ; 25T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type : Rapid Test CAT No : R0192C Clinical accuracy: 96.7% sensitivity, 93.8% specificity Analytical sensitivity: 100% positive detection rate at 1 ng/mL of pylori lysate antigen in fecal specimens Cross reactivity: no cross reactivity with the following organisms at â?¥ 1 x 108 org/mL: Acinetobacter calcoaceticus, Neisseria gonorrheae, Adenovirus, Neisseria meningitides, Enterococcus faecalis, Proteus mirabilis, Escherichia coli, Proteus vulgaris Hauser, Gardnerella vaginalis, Pseudomonas aeruginosa, Geotrichum candidum, Rotavirus, Haemophilus influenza, Salmonella Paratyphi A, �±-haemolytics streptococcus, Salmonella Paratyphi B, �²-haemolytic streptococcus, Salmonella Paratyphi C, Klebsiella pneumonia, Salmonella typhi, Moraxella catarrhalis Interference: No interference was seen with 5 mg/mL Tums�® Antacid, 1:20 Pepto-Bismol�® Antacid, 5 mg/mL Tagamet�® Antacid, 5% Barium sulfate, 5 mg/mL Prilosec Antacid, 12.5% Hemoglobin (tarry stool), or 1:20 Mylanta�® Antacid Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant Stool collection devices, each containing 2 mL extraction buffer Plastic droppers for transferring watery stool Package insert (instruction for use)