Product Details:
Number of Reactions(Preps)/Kit 22 Test
Brand Abbott
Usage/Application Hospital
Cat. No 710-000
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.
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.
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)
