Our commitment is to provide clean, reliable pumps that minimize problems for you and your patients.

Before we release a pump used to treat a patient, it goes through our 10-Point Quality Assurance Review. Our procedures exceed Government requirements and manufacturer’s guidelines, and include three separate surface wipe-downs, ultraviolet sterilization, volume accuracy and distal occlusion tests, program/history clearing, putting in a fresh set of batteries and more. In addition, we meet all F.D.A. “Device Tracking Requirements When Using Electronic Ambulatory Infusion Pumps.”

If any member of your facility wants to see a copy of our cleaning or testing protocols, please contact us. We’d be happy to provide you with a copy.