Jul 25, 2017 · Any modification by the laboratory to the Determine HIV–1/2 A g/Ab C ombo test or the FDA approved D etermine HIV–1/2 A g/Ab Combo test instructions will result in the test no longer meeting the requi rements for waived catego ry. A CLIA Certificate of Waiver is red to perform the test in a waived setting. The tests are performed when immediate actions are needed in situations of perinatal and occupational-exposure. Rapid HIV tests are simple to use with minimal equipment needed. The test can be performed by any health care worker with basic training. Test results are interpreted visually at the end of the reaction. 1 DETERMINE™ HIV-1/2 Ag/Ab COMBO Detection of p24 may be inhibited by biotin in the sample, causing false negative results in acute infection. Therefore, do not test samples from patients who HIV-1/2 Ag/Ab Combo Controls Catalog # 7D2628 Storage: Store at 2 to 8°C (36 to 46°F) Read this Package Insert and the Alere Determine™ HIV-1/2 Ag/Ab Combo Package Insert completely before using the product. Follow the instructions carefully when performing the test as not doing so may result in inaccurate Test Results. orthoclinicaldiagnostics.com *MicroTip Partnership Assay (MPA); Reagents and validated applications available directly from Ortho Clinical Diagnostics. Oct 28, 2023 · Depending on your test results, your doctor may recommend one of the following as a next step: Normal monitoring. If you're older than age 30, and your HPV test is negative and your Pap test is normal, you'll follow the generally recommended schedule for repeating both tests in five years. Colposcopy. .

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