FDA approves Smiths Medical Wireless Infusion Pump with 510(K) clearanceSeptember 26, 2011
September 26, 2011
Earlier this week, Smiths Medical announced their Medfusion 4000 gained 510(K) clearance from the Food and Drug Administration (FDA). Tommy Johns, VP for Global Product Management, described the Medfusion 4000 as “the next-generation advancement of the popular Medfusion 3500.”
This feature is backed up with the PharmGuard® management software. This software system allows wireless collection, management and Continuous Quality Improvement (CQI), accounting the patient’s infusion data for proper and accurate medication. In addition, the PharmGuard® Toolbox Medication Safety Software allows clinicians to create drug libraries that will be released to the Medfusion 4000 pumps. This eliminates the need for manual updates to the infusion pumps, which decreases the possibility of human error leading to medication miscalculation.
AIV provides replacement parts for the Medfusion 3500 and past models. To learn more about our Medfusion parts and repair options, visit http://www.aiv-inc.com/medex-medfusion-smith-infusion-pumps.html.
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