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CADRDIOSAVE Intra-Aortic Balloon Pump

The new CARDIOSAVE IABP incorporates a large state-of-the-art touchscreen display and is dramatically smaller, lighter and quieter than any pump the company has ever offered.

MAQUET Cardiovascular LLC, has announced U.S. Food & Drug Administration (FDA) 510(k) clearance and CE mark for its new CARDIOSAVE intra-aortic balloon pump (IABP). CARDIOSAVE is expected to be commercially available in the United States in January 2012.

The new CARDIOSAVE IABP incorporates a large state-of-the-art touchscreen display and is dramatically smaller, lighter and quieter than any pump the company has ever offered. The pump is being offered in two configurations: CARDIOSAVE Hybrid for routine in-hospital use and CARDIOSAVE Rescue for use in ambulances and aircraft.

For more information, visit ca.maquet.com [1].

Source URL (retrieved on 06/19/2013 - 11:36pm): http://www.surgicalproductsmag.com/product-releases/2011/11/cadrdiosave-intra-aortic-balloon-pump?qt-recent_videos=0&qt-recent_content=0

Links:
[1] http://ca.maquet.com/