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What are the applications that can be run on the AQUIOS CL system?

FAQs Product

Beckman Coulter‘s AQUIOS Tetra system tests for simultaneous identification and enumeration of T, B, and NK lymphocytes in whole blood are proven for reliability and precision and ideally complement the AQUIOS CL system. AQUIOS Tetra-1 and AQUIOS Tetra-2+ are for In Vitro Diagnostic Use. AQUIOS CL with Tetra-1 has been accepted for the World Health Organization list of prequalified in vitro diagnostic products.

For high burden HIV countries, Beckman Coulter offers the AQUIOS PLG (Pan-Leukocyte Gating) Panel that combines two fluorescent-labeled monoclonal antibodies in a single reagent formulation. It is intended “For In Vitro Diagnostic Use” for the enumeration of CD4+ absolute cell count and CD4+ lymphocyte percentage when used in combination with AQUIOS Flow-Count Fluorospheres as a single platform measurement.

The optional AQUIOS Designer Software opens the system for your own, user-defined tests.

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NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES. PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS The listed regulatory status for products correspond to one of the below: IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use." ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagent. Analytical and performance characteristics are not established." CE-IVD, CE: Products intended for in vitro diagnostic use and conforming to the In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746. (Note: Devices may be CE marked to other directives.) RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures." LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only." No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.