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Intelligent software supports safe operation and timely data transmission, safeguards patient data, and facilitates quick, convenient technical support,^‡ if needed.

• Predefined user-access profiles are password-protected to support tiered operator permission levels for safe system operation and patient data privacy.
• Smart Remote Services^§ identifies and diagnoses potential hardware issues, enabling rapid technical intervention and quicker resolution.
• Advanced QC interface provides comprehensive statistics, allowing the transmission of control results to the LIS.

Continuous random access and a fast average throughput of 65 tests^‡ per hour support flexible sample processing and rapid results.

• Flexible dilutions and automatic retesting can often be performed without re-accessing the primary sample.
• Sophisticated sample dilutions enable you to quickly add tests or retest samples.
• Samples and reagents can be loaded and reloaded continuously without interrupting the assay run.
• Integrated sample result traceability functions support intuitive historical data search and provide access to 2 years of onboard data.

High-capacity storage and automated features reduce hands-on time.

• Onboard reagent and control storage provides 24/7 operation, long onboard stability, and minimized operator intervention.
• High sample-loading capacity allows load-and-go processing.
• Positive bar-code ID of primary sample tubes minimizes manual steps and avoids sample mismatch.
• Automatic dilutions and repeat measurement of out-of-range high or low samples are performed without user intervention.

Proven nephelometric technology offers high precision and reproducibility that provide analytical advantages over turbidimetry in terms of precision and sensitivity.^1-4

• High-sensitivity testing with nephelometry is considered the industry’s “gold standard” and is recommended by the IMWG and ESMO guidelines.^5-7
• Wide initial measuring ranges and sophisticated antigen-excess pre-reaction protocols provide more-accurate results and fewer repeats.
• System detects specimen and reagent levels prior to processing to ensure accuracy of results.
• Graphical display of kinetic curves allows additional insight and advanced troubleshooting.

Innovative assays coupled with trusted and proven technologies support clinicians with reliable insight into disease determination and progression.

• N Latex FLC assay is the first immunoassay with clearance for evaluation of monoclonal gammopathies of undetermined significance (MGUS).^**,†�Ġ
• PROTIS® clinical decision support software^† consolidates patient test results into one simple report with algorithm-based interpretation of results to support physicians in clinical decision making.
• Lot-to-lot consistency ensures concordance of results, providing physicians with reliable insight into the progression of disease.
• More than 50 years of experience in protein analysis has led to longtime cooperation with IFCC in developing widely accepted standards.