| Place of Origin: | China |
|---|---|
| Brand Name: | Dewei |
| Certification: | ISO, CE |
| Model Number: | DWX-DOA |
| Minimum Order Quantity: | 5000 units |
| Price: | negotiable |
| Packaging Details: | 25test/box |
| Delivery Time: | in 20 days |
| Payment Terms: | T/T, D/P, , L/C, Western Union |
| Supply Ability: | 500,000pcs/day |
| Sample: | Whole Blood/Serum/Plasma | Usage: | Self Test Or Clinic Use |
|---|---|---|---|
| Type: | Strip/Cassette | Expiry: | 24 Months |
| Principle: | Chromatographic Immunoassay | Specificity: | 97.9% |
| Result: | Read In 10 Mins | Sensitivity: | 98.5% |
| High Light: | Hepatitis C Virus Rapid Diagnostic Kit,HCV Rapid Diagnostic Kit,Cassette rapid hcv test kits |
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Hepatitis C Virus (HCV) Rapid Diagnostic Kit Cassette Test Strip Serum/Plasma/Whole blood Specimen
【HCV INTRODUCTION】
Hepatitis C is a liver infection caused by the hepatitis C virus (HCV). Hepatitis C is spread through contact with blood from an infected person. HCV can cause both acute and chronic hepatitis infection, ranging in severity from a mild illness lasting a few weeks to a serious, lifelong illness. Hepatitis C is found worldwide. The most affected regions are Central and East Asia and North Africa.
【RAPID TEST INTENDED USE】
Hepatitis C Virus(HCV) Test Kit is a rapid, screening test for the qualitative detection of Hepatitis C virus antibody in human serum, plasma, or whole blood at specified cut-off levels.
【DIAGNOSTIC PRINCIPLE】
Chromatographic Immunoassay
【RAPID TEST SPECIMEN】
Serum/Plasma/Whole blood
【MAIN CONTENTS】
Test Cassette.
Disposable pipettes.
Buffer.
Instructions for use.
【STORAGE AND STABILITY】
The kit should be stored at 2-30°C until the expiry date is printed on the sealed pouch.
The test must remain in the sealed pouch until use.
Keep away from direct sunlight, moisture and heat.
Do not freeze.
Care should be taken to protect the components of the kit from contamination. Do not use it if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers, or reagents can lead to false results.
【APPLICABLE STANDARDS】
EN ISO 18113-1:2011, EN ISO 18113-2:2011, EN ISO 13612:2002, EN ISO 13640:2002.