ICU Medical receives FDA clearance for Plum Duo infusion pump and LifeShield infusion safety software, part of the new ICU Medical IV performance platform ICU Medical Inc. wants hospitals to question ...
The Food and Drug Administration sent a warning letter in early April to ICU Medical, alleging the company failed to submit premarket notifications for changes to infusion pumps. FDA inspectors found ...
The clinician-driven design of the precision system is the foundation of ICU Medical's (ICUI) long-term IV systems product road map that seeks to blend ease of use with proven medication delivery and ...
The U.S. FDA’s April 4, 2025, warning letter to ICU Medical Inc. cited the company for failure to file a new 510(k) for changes to software used in an infusion pump, but those changes may have been ...
New devices address infusion delivery variability and expand the ICU Medical IV Performance Platform. Unlike traditional pumps that rely on specific setups and conditions for accurate delivery, ...
A recall of nearly 62,800 replacement batteries used in several of ICU Medical’s infusion pumps has received the FDA’s Class I rating—the agency’s most serious, denoting a higher risk of serious ...
KLAS Research recognizes Plum 360 as 2021 Best in KLAS for Smart Pump EMR-Integrated, highlighting ICU Medical's pioneering efforts to advance industry standards for smart infusion pump ...
LONDON--(BUSINESS WIRE)--Technavio has been monitoring the global programmable infusion pumps market and the market is poised to grow by USD 487.81 million during 2020-2024 at a CAGR of almost 8% ...
New devices address infusion delivery variability and expand the ICU Medical IV Performance Platform. With these FDA clearances, ICU Medical is introducing its new category of precision IV pumps and ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results