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The intra- and inter-assay precision were calculated by running
three patient sera (negative, low positive, and high positive) in 24
replicates using two independent operators
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Company:
Date:
December 01, 2008
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The intra- and inter-assay precision were calculated by running
three patient sera (negative, low positive, and high positive) in 24
replicates using two independent operators.
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Company:
Date:
December 01, 2008
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The FirstVue H. pylori IgG Test is an (micro lateral flow) immunoassay assay for qualitative determination of antibodies to Helicobacter pylori (H. pylori) in human serum or plasma or whole blood for adults 18 years of age and older. This test is intended for use as an aid in the diagnosis of H. pylori infection in patients with clinical signs and symptoms of gastrointestinal disease.
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Company:
Date:
December 01, 2008
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An easy to use cassette test for H pylori, often responsible for stomach disorders, leading to ulcers and sometimes cancer. Helicobacter pylori is a bacterium that infects the mucus lining of the human stomach. Clinical pack, for serum or plasma. Immunoassay technology. CE Marked, FDA Approved cassette, more than 99 accurate. Lancet included.
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Company:
Date:
December 01, 2008
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The ImmunoCard® H. pylori enzyme immunoassay (EIA) is an in vitro qualitative procedure for the detection of IgG to Helicobacter pylori in human serum and plasma. Test results are intended to aid in the diagnosis of H. pylori infection. ImmunoCard® H. pylori may be performed in clinical laboratories and physician's offices.
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Company:
Date:
December 01, 2008
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Results in 6 minutes Easy-to-use, 4-step procedure
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Company:
Date:
December 01, 2008
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A rapid test for the detection of H pylori antibodies in human serum.
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Company:
Date:
March 11, 2009
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For the qualitative detection of urease associated with H. pylori in the human stomach and as an aid in the initial diagnosis and post-treatment monitoring in adult patients. Includes: Each kit includes one plastic tray with: Pranactin Citric drug powder (3g); self-adhesive bar-code labels; blue bag (for baseline sample); pink bag (for post-dose sample); transport bag; plastic straw; drinking cup; instructions; and package insert.
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Company:
Date:
December 01, 2008
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High sensitivity and specificity provide improved patient care
Easy-to-use assay provides results quickly
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Company:
Date:
December 01, 2008
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Includes: Complete with test devices, developer buffer, positive and negative controls, and instruction sheet Alert: Caution: Developer buffer and positive and negative controls contain sodium azide.Warning: Potential biohazardous material. Caution should be used when handling and disposing of samples at biosafety level 2.†
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Company:
Date:
December 01, 2008
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