Biovantion Inc.
Concentrate on IVD reagents
Add to Cart
One Step H. Pylori Test Device (Serum/Plasma)
INTENDED USE
The Dengue Ag NS1-IgM/ IgG rapid test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG anti– dengue virus, IgM anti-dengue virus and dengue antigen (Dengue Ag) in human serum, plasma or whole blood. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with dengue virus. Any reactive specimen with the Dengue Ag NS1-IgM/ IgG rapid test must be confirmed with alternative testing method(s).
| Product details | Description |
| Test Time | 5-20 miuntes |
| Packaging Specifications | 25 Test/Kit |
| Exp | two years |
| Manufacturer | BIOVANTION |
| Preservation method | Normal temperature |
| Assification | Class1 |
| Package | carton/box |
| Sample Type | Pharyngeal |
Features of H. Pylori Ag Reply test
1. Sensitive
2. Accurate
3. High quality
4. Economic price
5. Reliable and Easy to Use
PRECAUTIONS
1) For in vitro diagnostic use and professional use only.
2) Read the package insert instruction before use the kit.
3) Do not use beyond the expiration date which appears on the package label.
4) Do not open the sealed pouch, unless ready to conduct the assay.
5) Bring all reagents to room temperature (15°C-30°C) before use.
6) Do not use the components in any other type of test kit as a substitute for the components in this kit.
7) Haemolized blood may be used for the testing, but do not take precipitants.
8) Wear protective clothing and disposable gloves while assaying samples. Wash hands thoroughly after performing the test.
9) Handle all specimens as if they contain infectious agents. When the assay procedure is completed, dispose of specimens carefully after autoclaving them for at least one hour. Alternatively, they can be treated with 0.5 to 1% solution of sodium hypochlorite for one hour before disposal.
10) Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled.
11) Wear protective clothing and disposable gloves while assaying samples. Wash hands thoroughly after performing the test.
12) Handle all specimens as if they contain infectious agents. When the assay procedure is completed, dispose of specimens carefully after autoclaving them for at least one hour. Alternatively, they can be treated with 0.5 to 1% solution of sodium hypochlorite for one hour before disposal.
13) Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled.
11) Read result after 30 minutes may give erroneous results.
12) Do not perform the test in a room with strong air flow, ie. an electric fan or strong air- conditioning.
13) As with all diagnostic tests, a definitive clinical diagnosis should not be based on the results of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated.
14) Excess sample volume (>5µL) can give false positives.