Please provide your email address to receive an email when new articles are posted on . The FDA announced it designated a recall of intra-aortic balloon pumps due to problems related to fluid leak as ...
Getinge is recalling 4,338 intra-aortic balloon pumps after discovering fluid leaks that can lead to unexpected shutdowns or the inability to initiate therapy, the FDA said Dec. 16. The agency has ...
DUBLIN--(BUSINESS WIRE)--The "US Market Report for Intra-Aortic Balloon Pumps 2018 - MedCore" report has been added to Research and Markets' offering. An intra-aortic balloon pump system is used for ...
Flight nurses and paramedics at AirLift Texas bases in Waco and New Braunfels, have been trained to use the Getinge cardiosave hybrid balloon pump device during air transport, according to a July 17 ...
One way of assessing or assigning risk is to use a 'myocardium at risk' score. These scores help to systematically calculate the severity of CAD based on angiographic findings and also give an ...
A Japanese study of intra-aortic balloon pumps appears to indicate the devices do little to improve outcomes for patients with acute cases and may increase the chances of death. In the registry study ...
DUBLIN--(BUSINESS WIRE)--The "US Market Report for Intra-Aortic Balloon Pumps 2018 - MedCore" report has been added to Research and Markets' offering. An intra-aortic balloon pump system is used for ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback