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99.9% Dengue NS1 Rapid Test Infectious Disease Rapid Test Kits

Hangzhou Aichek Medical Technology Co.,Ltd
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99.9% Dengue NS1 Rapid Test Infectious Disease Rapid Test Kits

Brand Name : Aichek

Model Number : DEN-A01

Certification : CE

Place of Origin : China

MOQ : 5000 Test

Price : negotiable

Payment Terms : T/T

Supply Ability : negotiable

Packaging Details : 40box/carton

Storage : 2℃-30℃

Sample Type : Blood

User : Professional

Accuracy : 99.6% (97.7%-99.9%)

Certificate : CE ISO 13485

OEM : OEM customized packing avaliable

Formats : 25T/box 1T/box

After-sales Service : Available

Key words : Dengue NS1 Rapid Test

For the crowd : Preliminary screening of infected people

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Infection Disease Dengue NS1 Rapid Test with CE certificate Test Device

Product Name

Dengue NS1 Rapid Test

Formats Strip(3mm)Device(4mm)
Place of Origen China
Specimen Blood
Read Time 15 minutes
Shelf life 2 years
Package 25 device/box or 50 strip/Box
Storage 2℃-30℃

For professional in vitro diagnostic use only.

INTENDED USE

The Dengue NS1 Rapid Test Device is a lateral flow chromatographic immunoassay for the qualitative detection of dengue virus antigen (Dengue Ag) in human whole blood, serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Dengue viruses. Any reactive specimen with the Dengue NS1 Rapid Test Device must be confirmed with alternative testing method(s) and clinical findings.

SUMMARY AND EXPLANATION OF THE TEST

Dengue viruses, a family of four distinct serotypes of viruses (Den 1,2,3,4), are single-strained, enveloped, positive-sense RNA viruses. The viruses are transmitted by mosquitoes of the daytime-bitting Stegemyia family, principally Aedes aegypti, and Aedes albopictus. Today, more than 2.5 billion people living in the areas of tropical Asia, Africa, Australia, and the Americas are at risk for dengue infection. An estimated 100 million cases of dengue fever and 250,000 cases of life-threatening dengue hemorrhagic fever occur annually on a worldwide basis1-3.

Serological detection of IgM antibody is the most common method for the diagnosis of dengue virus infection. Lately, detection of antigens released during virus replication in the infected patient showed very promising result. It enables diagnosis from the first day after the onset of fever up to day 9, once the clinical phase of the disease is over, thus allows early treatment in placed promptly4.

The Dengue NS1 Rapid Test is developed to detect circulating dengue antigen in human whole blood, serum or plasma. The test can be performed by untrained or minimally skilled personnel, without laboratory equipment.

PERFORMANCE CHARACTERISTICS

Clinical Performance

A total of 114 patient samples from susceptible subjects were tested by the Dengue NS1 Rapid Test and by a commercial EIA. Comparison for all subjects is showed in the following table:

Dengue NS1 Rapid Test
Dengue Ag EIA Test Positive Negative Total
Positive 66 3 69
Negative 2 43 45
Total 68 46 114

Relative Sensitivity: 95.6%, Relative Specificity: 95.5%, Overall Agreement: 95.6%


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