Serum/Plasma Test

Hepatitis C Virus (HCV) Antibody Rapid Test Device (Serum/Plasma)

Rapid detection of Hepatitis C Virus antibodies in serum or plasma samples.

CE Certified
ISO 13485
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Main image of Hepatitis C Virus (HCV) Antibody Rapid Test Device (Serum/Plasma)

Why Choose reOpenTest Infectious Disease Kits?

Our tests are engineered for accuracy, reliability, and ease of use, ensuring confidence in every result.

Serum & Plasma Specific

Optimized for serum and plasma samples.

Fast Results

Provides results in 15-20 minutes.

Convenient Testing

Easy to use, one-step procedure.

Product Overview

The Hepatitis C Virus (HCV) Antibody Rapid Test Device is a qualitative immunoassay for the detection of antibodies to HCV in human serum or plasma. This rapid diagnostic test provides a convenient and efficient method for screening individuals for past or current HCV infection.

Technical Specifications

Detection Target HCV Antibodies
Sample Type Serum/Plasma
Methodology Immunochromatography
Detection Range Positive/Negative
Reaction Time 15-20 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect a serum or plasma sample.
  2. Apply the sample to the test device.
  3. Add the provided buffer solution.
  4. Read the results after 15-20 minutes.

Result Interpretation

Positive Result
Positive: The presence of a colored line indicates a positive result for HCV antibodies.
Negative Result
Negative: The absence of a colored line indicates a negative result.
Invalid Result
Invalid: If no control line appears, the test is invalid and should be repeated.

Frequently Asked Questions

The test demonstrates high sensitivity and specificity, minimizing the risk of false positive or negative results. Refer to the product insert for detailed performance characteristics.

Please check the product insert or contact us directly for the latest regulatory status.

No, this test detects the presence of antibodies, indicating past or current infection. Additional testing is required to determine the stage of infection.

Technical Documents

Download product inserts and brochures for detailed information.

No technical documents are available at this time. Please check back soon.

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