Basic Info.
Product Description
INTENDED USE
The Dengue IgG/IgM Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of dengue IgG and IgM antobody in human whole blood, serum, or plasma as an aid in the diagnosis of primary and secondary Dengue infections.
For professional in vitro diagnostic use only.
| Storage | 2~30 º C |
| Specimen | Whole Blood/Serum/Plasma |
| Component | Rapid Test + Buffer + Pipettes |
| Principle | Colloidal gold rapid tests |
| Reading | Within 15mins |
| Package | 40tests/box |
| Trademark | Dewei |
| Origin | China |
INTRODUCTION
Dengue viruses, transmitted by the mosquito, Aedes aegypti and Aedes albopictus mosquitoes, are widely distributed throughout the tropical and subtropical areas of the world. There are four known distinct serotypes (dengue virus 1, 2, 3 and 4). In children, infection is often subclinical or causes a self-limited febrile disease. However, if the patient is infected second times with a different serotype, a more severe disease, dengue hemorrhagic fever or dengue shock syndrome, is more likely to occur. Dengue is considered to be the most important arthropod-borne viral disease due to the human morbidity and mortality it causes. NS1 is a highly-conserved glycoprotein that is present at high concentrations in the sera of dengue-infected patients during the early clinical phase of the disease. NS1 antigen is found from the first day and up to 9 days after onset of fever in sample of primary or secondary dengue infected patients
MAIN CONTENTS
• A reaction test Cassette with desiccant.
• Buffer
• Disposable pipettes.
• Instructions for use.
STORAGE AND STABILITY
• Store at 2 ~ 30 º C in the sealed pouch for 24 months.
PRECAUTIONS
• For in vitro diagnostic use only.
• Do not use after expiration date.
• The test Cassette should remain in the sealed pouch until use.
• The used test Cassette should be discarded according to local regulations.
DIRECTION OF USE
INTERPRETATION
POSITIVE: Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
NEGATIVE: Only one colored band appears, in the control region (C). No apparent colored band appears in the test region (T).
INVALID: Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.
PRODUCT IMAGES
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CERTIFICATES
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