B. Braun Syringe Pump Includes Air and Road Transport in FDA 510(K) Indications for Use
IV Pump News June 26, 2018
B.Braun Medical received FDA Clearance for air and road transport for the Perfusor® Space 2nd Generation Syringe Pump.
The Perfusor® Space Syringe Pump was tested by registered, practicing nurses and anesthesiologists for over 100 hours and is intended for use on adults, pediatrics, and neonates by licensed medical professionals in healthcare facilities as well as air and/or road transport situations. It delivers intermittent or continuous delivery of fluids, medications, blood and blood products through intravenous, intra-arterial, subcutaneous, epidural, and enteral routes.
According to the B.Braun Medical’s Vice President of Marketing, Medical Device and Pharmaceutical Systems, the FDA 510(K) clearance allows healthcare professionals a wireless syringe pump that offers complete interoperability and versatility across various care and transport settings.
As the latest addition to the Synchronized Intelligence Infusion Platform, the pump aids clinicians in achieving 100% drug library compliance with minimized error. The pump offers complete integration with DoseTrac, DoseGuard, and AutoCOMPLETE™ Integrated EMR technology and has the same interface and wireless technology as the Infusomat® Space 2nd Generation large volume pump. Some key features of the Perfusor® Space 2nd Generation Pump include a compact design allowing for vertical stacking, automatic drive technology designed for accuracy and safety, an integrated piston brake to help prevent inadvertent bolus during syringe change, and a microprocessor to allow independent modularity to aid in preventing channel confusion and catastrophic pump failures.
AIV, Inc. is committed to providing high quality IV pumps, replacement parts, accessories and repair service for major infusion equipment manufacturers. Learn more about AIV’s wide selection of IV pump solutions at http://aiv-inc.com/iv-pump-parts-service.html.