HCV Hepatitis C Virus Antibody Rapid Test Kit

INTENDED USE

The reagent is used to detect the Hepatitis C Virus Antibody in serum / plasma / whole blood qualitatively. HCV is a single-stranded positive sense RNA virus, which belongs to the family of Flaviviridae. Hepatitis C caused by HCV is an infectious disease with liver as a target organ. The incubation period of hepatitis C virus infection was 2 to 26 weeks, most of the symptoms occurrs in 5 to 12 weeks after transfusion, on an average of 7.4 weeks. There is a long window period with an average of 70 days after the hepatitis C virus infection, however, some patients’ window period can be extended to 6~9 months or even longer. Hepatitis C virus antibody can be detected in most infections with a slow appearance. Generally positive results may occur 2~6 months after the attack, while some positive results occur 12 months later.

Sample Requirement

1. The reagent can be used for the serum, plasma and whole blood samples.

2. A serum / plasma / whole blood sample must be collected in a clean and dry container. EDTA, sodium citrate, sodium oxalate, heparin can be used as the anticoagulants. Detect immediately after collecting blood. If blood coagulation occurs, serum sample is suggested to use. Use the fresh whole blood samples.

3. Samples may be stored at 2-8℃ for 1 week prior to assay, and at -20 ℃ for 2 years. Frozen refrigerated samples should be recovered to room temperature before detection and thoroughly mixed. Repeat freeze and thaw for no more than 3 times. Samples exhibiting visible precipitates, stink or muddy should not be used. Centrifuged, filtered, or allowed to settle to obtain a clear sample for testing.

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