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 ...

We have learned that at the upcoming Medica 2008 (Nov. 19-22 in Düsseldorf, Germany), MAQUET GmbH & Co. KG is set to unveil the company’s latest circulatory bypass machine called CARDIOHELP, a device ...

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 ...

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 ...

(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 ...

WAYNE, N.J., Oct. 1, 2012 /PRNewswire/ -- MAQUET Medical Systems USA, a leader in extracorporeal life support (ECLS) systems, today announced that its CARDIOHELP System has been used successfully in ...

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 ...

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 ...

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 ...

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 ...

The heart-lung machine was approved for marketing in the US earlier this year for ground and air transportation and has been commercially available in many European countries for over a year. It is ...

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 ...