DXH 900 Body Fluids
DXH 900 Body Fluids
DXH 900 Body Fluids
With comprehensive body-fluids analysis available with the DxH 900 analyzer,
laboratories gain:
› Comprehensive BF analysis
The DxH 900 is capable of analyzing BF samples without any manual sample preparation.
› User-friendly software
Intuitive software with universally recognizable icons is easy to learn and use for the
laboratory technologist.
QUALITY RESULTS AND LABORATORY EFFICIENCY THROUGH
COMPREHENSIVE BODY FLUID ANALYSIS
› Sample-integrity monitoring
The DxH 900 uses blood detectors on all samples, minimizing the risk for spurious results linked
to air bubbles and partial aspiration.
› Capability for detecting minor bleeds
Sufficient sensitivity in BF mode to detect small amounts of blood due to minor bleeding.3
› Research Use Only capabilities
The DxH 900 provides the percent and number of mononuclear and polymorphonuclear cells
that have potential to provide additional information for manual reviews.*
› Reliable BF results
The DxH 900’s quality assurance procedures include three levels of BF controls, strengthening
confidence in results.
› Environmentally friendly system
The DxH 900 uses methanol-free and ethylene glycol-free reagents, thereby reducing
environmental impact and disposal costs.
The DxH 900 hematology analyzer: The right results, the first time
The DxH 900 empowers hematology decisions through near native-state cellular characterization,
ensures predictable costs through a 93% first-pass yield4 and maximizes staff time.
Discover the difference in quality results and laboratory efficiency through comprehensive BF
analysis. Visit www.beckmancoulter.com/DxH900.
References
1. Hematology analyzer Instructions for Use (IFUs) comparison.
2. Brown W et al. Validation of body fluid analysis on the Coulter LH 750. Lab Hematol. 2003;9:155–159.
3. Barnes P.W. et al. An evaluation of the utility of performing body fluid counts on the Coulter LH 750. Laboratory Hematology. 2004;10:127–131.
4. DxH series side-by-side results documentation.
*Research use only. Not intended for IVD use. Validation through a clinical trial is required to establish clinical utility.
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