Contact information Verified work emails, personal emails, and direct dials — unlocked in one click.
Work email
•••••@supersonicimagine.com
Personal email
•••••@•••••.com
Direct dial
+•• ••• ••• ••••
Free to start · No credit card required
Current company Supersonic Imagine
Medical Equipment Manufacturing · 84 employees · Founded 2005 · Aix-en-provence, France
Welcome to the official SuperSonic™ Imagine LinkedIn page. Connect with us to engage and network with industry leaders, and get the latest trends in ultrasound innovation and solutions. SuperSonic Imagine (SSI) specializes in ultrasound medical imaging. Manufacturing the flagship SuperSonic™ series of products, which feature the company’s exclusive UltraFast™ technology. UltraFast™ has given rise to new imaging modes that set the standards of care for non-invasive characterization of breast, liver and prostate diseases. The first groundbreaking UltraFast™ mode developed is ShearWave™ Elastography (SWE™), which enables physicians to view and analyze tissue stiffness, a vitally important factor in the diagnosis of many conditions. To date, more than 600 published articles have validated the diagnostic value. The company has more than ultrasound systems installed in over 80 countries, its main growth markets are China, the U.S. and the YouTube: Review our guidelines at http://bit.ly/SSI_Social Indications for Use: The SuperSonic Imagine Aixplorer MACH® 30 ultrasound diagnostic system and transducers are intended for general purpose pulse echo ultrasound imaging, Doppler fluid flow analysis of the human body, and soft tissue elasticity imaging. The Aixplorer MACH® 30 ultrasound diagnostic system is indicated for use in the following applications, for imaging and measurement of anatomical structures: Abdominal, Small Organs, Musculoskeletal, Superficial Musculoskeletal, Vascular, Peripheral Vascular, OB-GYN, Pelvic, Pediatric, Trans-rectal, Trans-vaginal, Urology, Neonatal/Adult Cephalic and Non-invasive Cardiac.(.) It is intended for use by a licensed personnel qualified to direct the use of the medical ultrasound devices. CE certificate no. 26415, FDA cleared K180572.