Clinical engineering plays a central role in planning for the replacement and acquisition of new capital equipment. The data you provide will directly impact the day-to-day operations and financial well-being of your organization for years to come. So what information do you need to provide, where do you get it, and who needs to receive it?
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Fujifilm Medical Systems will showcase its FDR D-Evo GL DR detector for single-exposure, long-length digital imaging at this week’s American Association of Orthopaedic Surgeons Annual Meeting in Orlando. The world’s first long-length digital radiography (DR) detector, the D-Evo GL has recently received FDA 510(k) clearance and will be readily available in the United States this spring.
Read MoreConquest Imaging, a supplier of Philips, Siemens, Toshiba, and GE Ultrasound equipment, announced that it was awarded a Federal Supply Schedule 65IIA contract by the VA National Acquisition Center. Under delegated authority by GSA, the VA manages multiple award contracts for medical equipment, supply, pharmaceutical, and service Schedule programs.
Read MoreAAMI has released a new technical information report examining the role of green practices in medical device manufacturing and selection. AAMI TIR65:2015, Sustainability of Medical Devices—Elements of a Responsible Product Life Cycle, provides general guidance on what sustainable practices look like for relevant stakeholders, including suppliers, manufacturers, distributors, and other healthcare technology professionals.
Read MoreFujifilm SonoSite Inc announced that it received the CE mark and 510(k) clearance for its new portable ultrasound system, the SonoSite Edge II. Designed for emergency medicine and critical care applications, the Edge II has advanced transducer technology that provides improved imaging for rugged environments.
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