Eitan Medical, a leader in advanced infusion therapy and drug delivery solutions across the care continuum, announced that its upgraded Sapphire infusion pump system software Rev15, which includes the infusion pump, administration sets and accessories, has received U.S. Food and Drug Administration (FDA) 510(k) clearance. The Sapphire infusion system is the company’s flagship infusion device, and is used across the U.S. within alternate sites, homecare markets, emergency medical services (EMS) and hospitals.
“The compact and robust Sapphire infusion pump is designed to deliver a wide range of therapies for varied clinical uses, such as saline, Total Parenteral Nutrition (TPN), lipids, IV medication, perineural medication, epidural medication, blood, and blood products, making it suited for complex and demanding medical scenarios,” according to a news release. “The pump’s smart technology includes a unique full color touch screen for intuitive and fast operation, built in safety mechanisms aimed to enhance patient safety, and advanced technology that helps minimize dosage errors and false alarms.
The most recent hardware and software upgrade adds a number of key improvements, utilizing the Sapphire family’s future-ready features.”
The new device features include:
“At Eitan Medical, we develop innovative and reliable technologies to provide a world-class user and patient experience via our drug delivery and advanced infusion solutions,” said Roger Massengale, CCO of medication delivery solutions at Eitan Medical. “For over a decade, the Sapphire infusion pump has established itself as an extremely capable and easy to use across the healthcare continuum. This clearance is an example of our continued dedication to innovation making our pumps easier to use for providers and safer for patients.”
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