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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.
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.
"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)
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.
A control lone in the “C” area of the result area indicates a valid result. A valid result indicates that a suitable sample was collected and that the test functioned properly. The control line will appear on all valid tests, whether or nor the result is negative.
Kit Control: Re-agents are available separately (Cat No. RBL 308-C). These are used to verify adequate test performance. Kit controls should be run once per shift by the test
The administrator of this test should first instruct the subject about the test and how to collect an oral fluid sample. Following which, the test device is then offered to the subject for the collection of the sample with reference to the guidelines appended below:
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Set the re-usable tans on a flat, level surface
more....The OraQuick® test is approved, and conforms to standards set forth by the U.S. Food and Drug Administration.
Such endorsements are testament to the high quality and standards of which OraQuick products are built upon.