HIV Professional Blood Test Cassette ALLTEST

Professional HIV 1/2 Antibody Rapid Test Kit

Medical-Grade Accuracy | >99.9% Correlation | Results in 10 Minutes

The HIV 1.2 Rapid Test Cassette is a CE-marked, professional-grade immunoassay designed for the rapid, qualitative detection of antibodies to Human Immunodeficiency Virus types 1 and 2 (HIV-1 and HIV-2).

Engineered for clinical precision, this test delivers reliable results using whole blood, serum, or plasma. It is an essential tool for hospitals, diagnostic labs, and public health screenings where speed and accuracy are paramount.

Important Notice: This is a professional in vitro diagnostic (IVD) product. It is intended for use by healthcare professionals and is not for home or self-testing.

Key Features & Clinical Benefits

• Dual Detection: Identifies antibodies for both HIV-1 and HIV-2.

• Versatile Sampling: Validated for use with venipuncture/fingerstick whole blood, serum, or plasma.

• Rapid Turnaround: Clear, actionable results in just 10 minutes.

• Certified Quality: CE 2934 certified, meeting stringent European IVD standards.

• High Stability: Simple cassette format requiring no additional instrumentation.

• Proven Reliability: >99% intra- and inter-assay precision for consistent performance.

Industry-Leading Accuracy

In comparative clinical evaluations against leading EIA and CMIA laboratory assays, this kit demonstrated a 99.9% overall accuracy rate.

Validated Performance: Extensively tested across HIV-1/HIV-2 subtypes, blood donor samples, and clinical specimens. The assay shows no cross-reactivity with common interfering substances or other markers such as Hepatitis, Syphilis, EBV, or CMV.

How to Use & Interpret

This membrane-based chromatographic immunoassay uses recombinant HIV antigens to capture specific antibodies. A coloured line at the Control (C) position ensures the test is functional.

• Positive: Two coloured lines appear (C and T).

• Negative: Only one coloured line appears at the Control (C) position.

• Invalid: No line appears at the Control (C) position.

Note: All reactive results should be interpreted alongside clinical findings and followed by confirmatory testing.

Technical Specifications

• Specimen Type: Whole Blood, Serum, Plasma

• Storage: 2–30°C (Do not freeze)

• Method: Rapid Chromatographic Immunoassay

• Certification: CE 2934 / IVD

• Format: Single-use Cassette