One of the benefits of interventional cardiology fellowship training is the exposure to new technology. Two newly approved devices—the CardioMems heart failure monitoring system (St Jude Medical) and ...

Getinge is recalling the Cardiohelp System emergency drive over concern that it can become stuck or hard to turn due to friction being generated in the handle attachment, according to a medical device ...

May 8 (Reuters) - The U.S Food and Drug Administration (FDA) on Wednesday advised healthcare facilities to move away from using Getinge's heart devices in patients as they faced safety and quality ...

Earlier this year, Getinge’s heart-lung support and permanent life support systems saw their CE marks be suspended over issues with their sterile packaging, and now, yet another of the Swedish ...

June 19, 2012 MAQUET Cardiopulmonary, a business unit of MAQUET Cardiovascular and a leader in extracorporeal life support (ECLS) systems, today announced that MAQUET CARDIOHELP® System has won three ...

SIOUX CITY | A new machine will give the hearts and lungs of patients in critical condition at Mercy Medical Center the support needed to rest and recover. The hospital purchased a $100,000 Cardiohelp ...

The Food and Drug Administration in a letter Wednesday told healthcare providers and facilities they should stop using certain Getinge cardiovascular medical devices. Getinge has initiated 20 recalls ...

WAYNE, N.J., April 28, 2011 /PRNewswire/ -- MAQUET Cardiovascular today announced that the U.S. Food and Drug Administration has granted the company 510(k) clearance to market its CARDIOHELP System in ...

SIOUX CITY | Mercy Medical Center purchased a $100,000 Cardiohelp system in December to give the hearts and lungs of patients in critical condition the support needed to rest and recover. This ...

Blessing of technology for patients suffering from oxygen shortage during surgery Sharjah: It’s a blessing of technology for all patients who are suffering from complication due to an oxygen shortage ...

(Reuters) -The U.S Food and Drug Administration (FDA) on Wednesday advised healthcare facilities to move away from using Getinge's heart devices in patients as they faced safety and quality concerns ...