Biovantion Inc.
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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 Detail | Description |
| Packaging Specifications | 50 tests/box |
| Country Of Origin | China,BeiJing |
| Detection Limit | 24 months |
| Storage | 4-30℃ |
| Specimen | serum, plasma, whole blood,fingertip blood |
| Instrument classification | Class I |
| Product Type | Repid Test |
| Accuracy | 99.9% |
| Application | Hospital, Medical Center,self |
STORAGE AND STABILITY
All reagents are ready to use as supplied. Store unused test device unopened, preferably at 2°C-30°C. Do not expose the kit over 40°C. Do not freeze the kit. The positive and negative controls should be kept at 2°C-8°C. If stored at 2°C-8°C, ensure that the test device is brought to room temperature before opening. The test device is stable through the expiration date printed on the sealed pouch if it is stored at 2°C-30°C.