ICU Medical Receives FDA Approval for Plum Duo™ Infusion Pump and LifeShield™ Infusion Safety Software

ICU Medical has received 510(k) regulatory clearance from the U.S. Food and Drug Administration (FDA) for the Plum Duo infusion pump with LifeShield infusion safety software which will be available in the U.S. in early 2024.

The Plum Duo pump is the newest addition to ICU Medical’s portfolio of infusion devices and builds on the precise delivery of the unique cassette technology in the Best in KLAS award-winning Plum 360™. It features a large color touch screen with a highly intuitive user interface and two channels capable of delivering up to four compatible IV medications.

LifeShield infusion safety software is a unified cloud-based software suite that provides advanced new tools for comprehensive drug library management. It fosters collaboration by enhancing clinicians’ ability to access, process and quickly share information across an entire enterprise or health system.

“Receiving FDA clearance for the Plum Duo pump and LifeShield software is the first step in realizing ICU Medical’s long-term vision of bringing customers best-of-breed devices with a shared platform and user experience,” said Dan Woolson, corporate vice president and general manager of ICU Medical Infusion Systems. “We are proud of this milestone and look forward to bringing our next-generation Medfusion™ and CADD™ products to the LifeShield platform, creating the most complete, precise, and technologically advanced infusion systems in the industry for our customers and their patients.”