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Radiaction Medical Announces the Latest Food and Drug Administration 510(k) Clearance for its Novel, Automated Radiation Shield System, Highlighting U S Expansion

Alexa as EKG; Post-COVID Clot Prevention; Retinal Artery Stroke Guidance

email article Smart home speakers like Amazon Echo can be used to monitor heart rhythms by sonar, researchers report in Communications Biology. The ACTIV-4 Convalescent trial is now underway testing apixaban (Eliquis) for thromboprophylaxis after discharge for moderate-to-severe COVID-19, the NIH announced. Even if heart failure stabilizes without improving on cardiac resynchronization therapy, 5-year prognosis is much better than was thought, suggesting that the current convention of nonresponder classification should be modified, according to a REVERSE trial analysis. ( JACC: Clinical Electrophysiology) The 4PEPS tool safely ruled out pulmonary embolism solely on clinical criteria and optimized D-dimer measurement, while substantially reducing imaging tests. (

ControlRad Announces FDA Clearance for ControlRad Select

ControlRad Announces FDA Clearance for ControlRad Select ATLANTA, March 4, 2021 /PRNewswire/ ControlRad, Inc., a privately held medical technology company focused on dramatically reducing unnecessary radiation exposure during fluoroscopically guided procedures, has announced the U.S. Food and Drug Administration (FDA) 510(k) clearance to market ControlRad Select. The technology utilizes proprietary semi-transparent filters, a user-interface tablet, and image processing algorithms, which are retrofitted onto customers existing Siemens Artis zee interventional imaging systems. In preparation for the commercialization efforts, ControlRad has entered into an exclusive agreement with Boston Scientific Corporation to sell the ControlRad Select technology. With the FDA clearance and the reach of the global medical device sales team, every cath, EP, and IR lab in the country that has a Siemens Artis zee will now have the opportunity to reduce their radiation dose by 85%

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