• DPP HIV 1/2 - Nordic Tests ApS
  • DPP HIV 1/2 - Nordic Tests ApS
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Nordic Tests ApS

Chembio DPP HIV 1/2 Assay

Chembio DPP HIV 1/2 Assay

1.990,00 DKK
1.990,00 DKK
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Chembio DPP® HIV 1/2 Assay

CE-marked and FDA-approved rapid HIV test – accurate results in just 15 minutes.

The DPP® HIV 1/2 Assay uses Chembio’s patented Dual Path Platform® technology to detect antibodies to HIV-1 and HIV-2. The test is flexible, user-friendly and validated for professional point-of-care use.

For professional use only. Not for self-testing.

  • Result in approx. 15 minutes
  • Sensitivity and specificity close to 100%
  • Sample material: finger prick, venous whole blood, serum, plasma – and in some versions oral fluid
  • CE-marked in Europe • FDA-approved and CLIA Waived in the USA
Contents:
20 cassettes, 20 oral swabs, 20 sample loops, 20 buffer dropper bottles, 1 migration buffer vial

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Chembio DPP HIV 1/2 Assay
Chembio DPP HIV 1/2 Assay
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Produktinformation

Produktbeskrivelse

Chembio DPP® HIV 1/2 Assay – rapid, precise and professional HIV diagnostics

The DPP® HIV 1/2 Assay is a modern rapid test developed by Chembio Diagnostic Systems for the detection of antibodies to HIV-1 and HIV-2. It is based on the company’s patented Dual Path Platform® (DPP®) technology, which ensures efficient separation of sample and reagents and thereby higher signal strength and clearer results than traditional lateral flow tests.

Function and method

The test requires only a small sample volume (approx. 10 µl) and can be used with finger-prick blood, venous whole blood, serum or plasma. In some versions (USA), oral fluid is also approved. The procedure is simple: the sample is applied to the test cassette together with buffer, after which the result can be read after about 15 minutes. A control line indicates that the test has been performed correctly, and the use of the Chembio DPP Micro Reader enables objective and quantitative reading.

Performance and accuracy

Both the US (FDA-approved, CLIA waived) and the European (CE-marked) versions have shown sensitivity and specificity close to 100%. The test has been validated across different populations and sample types and meets WHO and FDA performance requirements for HIV diagnostic rapid tests.

Advantages


  • Reliable results in 15 minutes

  • Very small sample volume required

  • Multiple sample types supported (finger-prick, venous blood, serum, plasma – possibly oral fluid)

  • Option for visual or instrument-based reading

  • CE-marked for use in Europe, FDA-approved in the USA

Use

The DPP® HIV 1/2 Assay is intended for professional use in clinics, hospitals, laboratories and outreach programmes. It is particularly suitable in settings where rapid and accurate test results are crucial for patient counselling and initiation of treatment.

Download the instructions for use here

Bestillingsinformation

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