Procleix® HIV Assay
This assay is only available as part of a panel and cannot be ordered individually.
The Procleix Ultrio Assay is a qualitative in vitro nucleic acid assay system to screen for human immunodeficiency virus type I (HIV-1) RNA in plasma and serum specimens from individual human donors, including donors of whole blood, blood components, and source plasma, and from other living donors. This assay is not intended for use as an aid in diagnosis of infection with HIV-1. The test has been cleared or approved for diagnostic use by the U.S. Food and Drug Administrations.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above. The CPT codes provided are based on Viracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.