Can I run my own user-defined assays on the AQUIOS CL system?

Absolutely. The optional AQUIOS Designer Software allows you to create user defined protocols, compensation matrix, sample preparation steps, and QC features on the AQUIOS CL flow cytometer. This lets you run the applications you want to run, while enjoying the automation benefits that AQUIOS can provide. Together with our Contract Manufacturing or Custom Design* Services of user-defined reagents, we provide a unique combination of sample preparation, barcoded user-defined reagents, data analysis and automated tracking of QC functionalities - all in one compact platform, and tailored to your specific needs (AQUIOS Designer Software is not available in all countries. Please consult your local Beckman Coulter representative for details).

* Custom Design Services products are for Research Use Only. Not for use in diagnostic procedures

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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.