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Home » FDA clears portable blood, IV fluid warmer from Mequ

FDA clears portable blood, IV fluid warmer from Mequ

June 7, 2024 By Sean Whooley

Mequ IV_Blood warmer system
The M Warmer and power pack. [Image courtesy of Mequ]
Mequ announced today that the FDA granted 510(k) clearance to its M Warmer system, a portable blood and IV fluid warmer platform.

The Copenhagen, Denmark–based medtech company offers the warmer for both military and civilian use. It features a portable, user-friendly design that enables the warming of blood and IV fluids regardless of location. That includes point of injury, during transport and in the hospital.

Mequ originally developed the M Warmer system in collaboration with the Danish military and Technical University of Denmark. It aimed to reduce hypothermia and improve the survival and recovery rate of severely injured patients.

According to a news release, Mequ conducted numerous trials with U.S. military units and helicopter emergency medical services.

Get the full story at our sister site, Drug Delivery Business News.

Filed Under: 510(k), Blood Management, Drug Pumps, Drug-Device Combinations, Food & Drug Administration (FDA), Regulatory/Compliance Tagged With: Mequ

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About Sean Whooley

Sean Whooley is a senior editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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