(1)The Dengue IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum, or plasma as an aid in the diagnosis of primary and secondary Dengue infections.
(1)The test device contains Dengue antigen-coated particles and ligand anti-human IgM. Anti-human IgG and anti-ligand are coated in the test line regions.
(1)For professional in vitro diagnostic use only. Do not use after the expiration date.
(2)Do not eat, drink or smoke in the area where the specimens or kits are handled.
(3)Do not use the test if the pouch is damaged.
(4)Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout testing and follow the standard procedures for proper disposal of specimens.
(5)Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are being tested.
(6)The used test should be discarded according to local regulations.
(7)Humidity and temperature can adversely affect results.