Flexible testing capabilities, powerful cytometry software and a user-friendly interface. The CXP analysis software improves sample-to-result times and throughput. CXP provides automatic daily monitoring of system performance, simplifying daily quality control recording. Built in Levy-Jennings plots are updated with each QC run for constant quality monitoring. The integrated product log keeps track of lot numbers and expiration dates for compliance for regulated laboratories. Customized panel reporting is available to tailor reports. Each report can include user-selected statistics and plots from the panel. Output can be made via a printed page or PDF documents to e-mail to offsite laboratories easily. Bundle priced and licensed for three users, making it convenient for small labs. Requires Windows 7.

Specifications

Platform FC500
Regulatory Status nMD
UNSPSC 41116015

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 Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
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.