These infusion system replacement batteries were recalled because a defect has diminished how long they can be used to run the system, which may cause the system to shut down an ongoing infusion.
Avation Medical announced that its non-invasive, bladder control therapy device, Vivally, received U.S. FDA 510(k) clearance.
As a biomed, bringing your talent to a developing world hospital that is struggling for sound medical equipment can be an intensely satisfying experience. For those who are thinking about making a medical mission trip to the developing world for the first time, partnering with an organization that can help prepare supplies and contacts is key to a successful experience.
The reduction in duration of hospital stays and cost-of-care is driving growth of the home infusion therapy market.
Invictus Medical has submitted a De Novo application to the FDA for its Neoasis incubator-based active noise control device.
Currently valued at $14.9 billion, the global anesthesia devices market is slated to exhibit a compound annual growth rate of 7.6% by 2030.
Baxter has issued a medical device correction for the Life2000 Ventilation System, citing the potential for patient oxygen desaturation events due to improper use with third-party oxygen concentrators, which may cause patient harm or even death.