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ACUSON S2000 Ultrasound System - Technical Specifications
Superior architecture, advanced clinical applications and high resolution transducers deliver never before seen detail.
- Enhanced anatomic border definition and improved tissue contrast with Advanced SieClear™ spatial compounding
- Reduced speckle/noise and enhanced borders both in 2D and volume (3D/4D) modes with Dynamic TCE™ tissue contrast enhancement technology
- Improved slice thickness, image uniformity, and contrast resolution with the high density transducer technology on the 18L6 which incorporates twice the elements with half the space
Innovative Applications
The ACUSON S2000 system is versatile and supports a complete suite of transducers for virtually every clinical application. Tranducers use Siemens best-in-class proprietary micro-pinless (MP) transducer connector technology, optimized for high-frequency imaging. You can go beyond conventional modes of 2D, 3D, 4D, and Doppler imaging to support a broad range of today’s most cutting-edge clinical applications:
- Unique core acoustic technologies and state-of-the-art design provide precise details of complex pathology and subtle lesions in examinations
- Virtual Touch™ applications* implement ARFI imaging technology to provide both qualitative regional and quantitative spot assessments of deep tissue stiffness
- eSie Touch™ elasticity imaging software utilizes gentle manual compression to display high resolution relative tissue stiffness
- Cadence™ contrast pulse sequencing technology (CPS)** provides a non-linear imaging technique to effectively separate and display tissue or contrast; excellent for lesion detection and characterization
- Contrast™ Dynamics software provides an extra level of diagnostic data through visual quantification of time course of contrast enhancement in images
*Virtual Touch applications are not yet commercially available in the USA.
**At the time of publication, the U.S. Food and Drug Administration has cleared ultrasound contrast agents only for use in LVO. Check the current regulation for the country in which you are using this system for contrast agent clearance.
