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Intuitive, icon-based user interface makes method setup & workflow maintenance easy
Provides full control over complex tip movements
Can be integrated with third party devices
21 CFR Part 11 compliance in regulated environments
Ease of Operation
Simple point-and-click interface
Step-by-step guidance for labware placement
Easily toggle between current running applications
Vary runs without programming
“Lock down” status for protection of validated methods
Captures necessary data for process validation & reproducible results
Integrates with LIMS systems to import work orders & export data
Transfers data between methods for generated runs, labware & sample reports
Selectable actions during execution based on real-time sample data
Quickly select pipetting techniques, liquid types & deck layouts from drop-down menus
Scan plates & import sample IDs based on plate barcodes
Track sample IDs throughout the run for maximum accuracy
Validate methods in real-time with a simple to use visual editor
Software Solution Add-ons
Method Launcher provides the ability to select, set up, run and track methods in real-time
SAMI EX creates planned schedules with the benefits of an optimized, predictable static schedule
SAMI Process Management organizes SAMI EX methods in an easy-to-use calendar tool
DART 2.0 (Data Acquisition and Reporting Tool) gathers data and synthesizes runtime information to capture each manipulation of a sample
PowerPack uses advanced tools to make programming data-intensive methods easy Technical Documents
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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 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.