Home Or Health Clinic Tropical Disease Dengue IgM Detection Test

One Step Dengue IgG & IgM Test(Serum / Whole Blood)

INTENDED USE

The Dengue IgM and IgG Combo Rapid Test is a qualitative test for the detection of IgM antibodies to dengue virus in human serum, plasma or whole blood. This test is for in-vitro diagnostic use only.

Features of Hbasg Elisa Kit:
1. Sensitive

2. Accurate

3. High quality
4. Economic price

5. Reliable and Easy to Use

IGG Positive.

The control line and IgG line are visible on the test stripe. The test is positive for IgG antibodies. This is indicative of a past dengue infection.

IgM Positive

The control line and IgM line are visible on the test strip. The test is positive for IgM antibodies. This is indicative of a primary dengue infection.

IgM and IgG Positive.

The control line, IgM and IgG lines are visible on the test strip. The test is positive for IgM and IgG antibodies. This is indicative of a secondary dengue infection.

Negative Test Result

The control line is the only line visible in the test device window. No IgG or IgM antibodies were detected. The result does not exclude dengue infection. If symptoms persist, a new sample should be drawn from the patient in 3-5 days and then should be retested (see the limitations section).

Invalid Test Result

If the control line does not appear in the test device window, the test results are INVALID regardless of the presence or absence of line in the test region of the device window. Repeat the test using a new device.

Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro virus, Parvo virus test kits, our products include rapid test cassette and Elisa kits.

All our products have been registered in National Medical Products Administration of China, in year 2020 we get Certificate of ISO 13485:2016 – QUALITY MANAGEMENT SYSTEMS FOR MEDICAL DEVICES from SGS. More importantly, we have awarded the registration certificate from National Medical Products Administration for Diagnostic Kit for IgM Antibody to COVID-19 and IgG antibody to COVID-19 during the outbreak in China, and also we developed COVID-19 Antigen test ; Neutralizing Antibody Test, these products selling well all overthe world