Feces Norovirus Rapid Test 20pcs Antigen Test Kit Colloidal Gold

Rapid Test for Detection of Norovirus antigen(Colloidal Gold)

Catalog No.:

INTENDED USE

Bioneovan Rapid Test for Detection of Norovirus antigen(Colloidal Gold) is an in vitro immunoassay for the qualitative determination of the detection of norovirus in human feces specimens in one step. As an auxiliary diagnosis of acute viral gastroenteritis, it quickly diagnoses the pathogen for disease, avoids the spread of hospitals or communities and reduces the need for unnecessary antibiotic therapy.

TEST PROCEDURE

If the kit is kept in the refrigerator, return the kit to room temperature before use.
1. Unscrew the cap, remove the picking screw, take the sample from the feces (about 100mg), place it in the picker with the sample diluent, and tighten the cap.
2. Shake and mix, and screw the top cap of the toilet.
3. Place the test card on a flat surface, vertically and slowly add 2-3 drops of the mixed sample (about 80 μl) to the center of the test card loading end.

5-15 minutes of interpretation. After 15 minutes, the interpretation is invalid.

INTERPRETATION OF RESULTS

C-line color development only: negative; C line, II line color development: Norovirus antigen (GII) positive; C line, I line color development: Norovirus antigen (GI) positive; C line, II line, I line color development: Norovirus antigen (GII) and Norovirus antigen (GI) are positive at the same time; only R line or A line color: invalid; C line, R line A line are not color: invalid.

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