January 28, 2008 – Medtronic Inc. has launched a clinical trial to confirm the safety and efficacy of the Medtronic EnRhythm MRI SureScan pacing system, a pacemaker system to be developed and tested specifically for safe use in Magnetic Resonance Imaging (MRI) machines under specified scanning conditions.

January 28, 2008 - Arbor Surgical Technologies Inc. closed a $20 million dollar Series C financing round led by Medtronic Inc. as part of a licensing agreement, providing Medtronic with manufacturing, marketing and distribution rights to Arbor’s advanced trilobal pericardial valve technologies.

January 28, 2008 - MediGuide signed an agreement with Medtronic for co-development of medical positioning system-enabled products, providing Medtronic products with GPS-like navigation capabilities to enhance various procedures.

January 28, 2008 - Toshiba America Medical Systems Inc. said today the FDA cleared the new open-bore 1.5T Vantage Titan MR system, which will be commercially available in the first quarter of 2008.

The open-bore of the Vantage Titan is 18 percent larger than other 1.5T systems on the market, featuring a large 71-centimeter patient aperture.

Monitoring system maker Mennen Medical said an additional monitor, the VitaLogik 4000 Series, will soon be available for monitoring requirements in neonatology, pediatrics, cardiology, ICU, OR, and ER.

The product is available in two versions. The noninvasive VitaLogik 4000 and the invasive VitaLogik 4500 and has FDA clearance and CE mark.

MEDecision Inc. introduced Alineo, a collaborative healthcare management platform for addressing case management, disease management and utilization management.

GE partnered with anesthesiologists, emergency medicine physicians and other fields of medicine to design new editions of its LOGIQ e compact and a new edition of the LOGIQ Book XP Enhanced compact, as part of its Breakthrough 2008 ultrasound releases. GE introduced these dedicated systems with features and software streamlined for emerging care areas of ultrasound.

The FDA granted Ethicon Inc. an expanded indication for EVICEL Fibrin Sealant (Human), which is one of the first fibrin sealants available as an adjunct to hemostasis for use in surgery, when control of bleeding by standard surgical techniques is ineffective or impractical.

Cheetah Medical Inc. said the FDA cleared for marketing the Reliant, a portable cardiac output monitor that provides a noninvasive window to cardiac and hemodynamic function.

A new line of functional and comfortable tracheostomy tube holders that are offered with designs for babies, kids and teens is being introduced by Dale Medical Products Inc. of Plainville, MA

Dale PediPrints Tracheostomy Tube Holders feature the new PediDucks, PediStars and Blue designs for babies, kids, and teens which are printed onto latex-free neckbands that are moisture repellent and ensure a snug fit. Providing fastener tabs that are shaped to easily fit into the flange of any size trach tube, these trach holders have rounded hook-and-loop back tab fasteners for sizing.

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