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ORAQuick HIV Test kit is the only Rapid Test kit approved by USFDA!

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OraQuick Rapid HIV 1/2 Antibody Test

INTRODUCTION OF ORAQUICK

The OraQuick® Rapid HIV 1/2 Antibody Test is a visually read, qualitative immunochromatic test.

The OraQuick® Rapid HIV 1/2 Antibody Test simplifies test procedures and provides both individuals and practitioners a fuss free and time efficient alternative to traditional HIV screening tests. All that is required from the patient for the administration of the test is either an oral fluid sample, a small drop of blood from the finger, or a small sample of blood from the vein.

Because the OraQuick® is rapid test, results can be obtained within a mere 20 minutes, of which is instrumental in reducing patient stress and anxiety, often induced by longer waiting periods, as well as blood taking.

WHAT IS ORAQUICK RAPID HIV 1/2 ANTIBODY TEST USED FOR?

The OraQuick® Rapid HIV 1/2 Antibody Test is used for the detection of antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2). A sample in one of the following forms: human oral fluid, fingerstick whole blood, venipuncture whole blood, or plasma specimens is required for the administration of the test.

Testimonials

"Fast Quick and easy to use. what more can i say?" - Mike L USA (Name reduced for confidentiality)

"The kits are easy to use and it is not messy. My results came in 20mins and i felt great!" - Scott A. USA (Name reduced for confidentiality)

"The delivery was fast, it came almost the next day for my urgent order. i am doing the test monthly now to be safe for for peace of mind" - Md. A.A.M (UAE) (Name reduced for confidentiality)

HOW ACCURATE IS IT?

Based on a study conducted in the US, sensitivity is 99.3% and specificity is 99.8% using oral fluid (Saliva); and sensitivity is 99.6%.

OraQuick® Rapid HIV 1/2 Antibody Test promises speedy yet laboratory accurate results for individuals who undergo the OraQuick® Rapid HIV 1/2 Antibody Test.

OraQuick® Rapid HIV 1/2 Antibody Test is approved by the US Food and Drug Administration.