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June 7, 2011 – At SNM 2011, Siemens Healthcare demonstrated how users of the Symbia S and Symbia T series, single-photon emission computed tomography (SPECT) and SPECT•CT systems, respectively, are taking advantage of IQ•SPECT, to dramatically reduce the length of imaging protocols. A field-upgradeable combination of hardware and software, IQ•SPECT is helping nuclear cardiologists cut the cardiac imaging protocol from approximately 20 minutes to less than five minutes. These shortened exams enable a sustainable approach to nuclear cardiology that potentially enables decreased radiation dose to patients, assists to make the procedure more tolerable for the elderly, provides high quality diagnostic information, and allows users to better utilize an imaging resource that is hampered by limited availability of the key radiotracer.

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June 7, 2011 - CoActiv introduces Exam-Browser, a cloud-based, zero-footprint, universal clinical viewer that enables anywhere, anytime review of medical images and reports. With the new Exam-Browser, CoActiv hospital and imaging center clients storing images in CoActiv’s vendor-neutral Exam Vault cloud-based archive can enable users to view and manipulate exams with ultra-fast speed from virtually any browser-enabled computer or mobile device, anywhere in the world, quickly and securely. This includes Windows, Linux and Mac PCs as well as most Smartphones and tablets including the iPhone, iPod, iPad, Android phones, HP Slate, Motorola Xoom, T-Mobile Slate, CoActiv Exam-Pad, Samsung Galaxy, Blackberry Torch and more. The system operates using wired, Wi-Fi or 3G/4G mobile Internet connectivity.

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June 7, 2011 – MIM Software Inc. announced the VueMe App for iPad, iPhone and iPod touch is now available on the App Store. This new app, designed specifically for patient use, allows patients to view diagnostic images sent to them from their doctors, and to share these images, if needed, with specialists. The launch of VueMe comes on the heels of Mobile MIM, MIM Software's original remote diagnostic imaging app for physicians.

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June 7, 2011 – MIM Software Inc., a global provider of medical imaging software, has released MIMcloud 2.0 worldwide. MIMcloud provides an easy, convenient, and secure way for physicians and patients to transfer images.

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June 6, 2011 - TeraRecon Inc. highlighted Integration and Interconnectivity of the iNtuition enterprise advanced visualization solution to imaging and informatics professionals assembled for the Annual Meeting of the Society of Imaging Informatics in Medicine (SIIM), June 2-5, 2011.

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June 6, 2011 –Intelerad Medical Systems announced the availability of its Multi-Method Reporting module along with the new IntelePACS 4.3 release, which provides radiologists access to voice recognition in their reporting workflow. Designed to accommodate the way radiologists naturally read and report studies, Intelerad’s Multi-Method Reporting blends dictation, voice recognition and structured report templates together in a single, streamlined interface and workflow.

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June 6, 2011 – AngioDynamics has expanded its VenaCure EVLT System product offering with the global launch of the new VenaCure 1470nm laser to treat varicose veins with greater energy efficiency.

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June 6, 2011 - AccessClosure Inc announced an exclusive agreement with Biosensors International for the distribution of the Mynx Vascular Closure Device throughout the United Kingdom, Switzerland and France. The extravascular Mynx device, designed for patient comfort while providing hemostasis without sutures or implants, will be sold as part of Biosensors' interventional cardiology product range.

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June 3, 2011 – New long-term data from the DIVERGE study, presented at EuroPCR 2011, showed that the use of the Axxess drug-eluting stent (DES) for the treatment of complex coronary bifurcation lesions resulted in low levels of both major adverse coronary events (MACE) over a three-year period. Axxess is a self-expanding bifurcation stent that releases Biolimus A9 from an abluminal biodegradable polymer coating.

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June 3, 2011 - IDEV Technologies announced that data from a long lesion study of 182 patients with significantly diseased superficial femoral arteries and popliteal arteries showed high patency rates and no stent fractures after treatment with the Supera Veritas Peripheral Vascular Stent System. The data were presented at the Vaatdagen 2011 (Vascular Days) Conference based on analysis by Andre Molenaar, M.D., and Peter Haarbrink, M.D., interventional radiologists at Canisius-Wilhelmina Ziekenhuis (CWZ) hospital, a leading teaching and high volume medical center in Nijmegen, The Netherlands.

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June 3, 2011 – At the Society of Imaging Informatics Management (SIIM) meeting, Novarad introduced NovaCardio, a fully integrated cardiac picture archiving and communications system (CPACS) image and information management system. It offers fast and efficient clinical workflow, powerful features and is accessible anywhere viewing and reporting.

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June 3, 2011 - Research presented at the International Federation of Clinical Chemistry Congress and Laboratory Medicine showed that using a lower diagnostic threshold for troponin improves clinical outcomes and patient survival in patients with suspected acute coronary syndromes. Troponin is a protein found inside heart cells that is released when they are damaged by ischemia or reduced blood supply.

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June 3, 2011 -- Maquet Cardiovascular announced that the U.S. Food and Drug Administration (FDA) has granted the company 510(k) clearance to market its CardioRoot aortic graft in the United States. A one-piece design, aortic root graft, CardioRoot will be used by vascular and cardiovascular surgeons to surgically repair or replace diseased and damaged aortae. CardioRoot is now commercially available in the United States.

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June 3, 2011 – European CE mark approval was granted to expand use of the VerifyNow point-of-care P2Y12 test platelet reactivity test to identify patients who are poor-responders to antiplatelet therapy (e.g. clopidogrel).

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June 2, 2011 – The U.S. Food and Drug Administration (FDA) this week is warning medical professionals and U.S. medical device vendors to beware of possible safety concerns and radioactive contamination of medical devices and components coming from Japan.

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