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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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11 records meeting your search criteria returned- Product Code: KFM Product Problem: Device Inoperable Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ABIOMED, INC. IMPELLA 06/28/2018
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 12/01/2014
ABIOMED EUROPE, GMBH (GERMANY) IMPELLA RECOVER LP2.5 PERC CARDIAC SUPPO 09/18/2014
ABIOMED, INC. IMPELLA 08/26/2014
ABIOMED, INC. IMPELLA 06/26/2014
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP 04/11/2014
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP 04/11/2014
CARDIAC ASSIST, INC. TANDEMHEART PUMP 04/10/2014
MAQUET CARDIOPULMONARY AG ROTAFLOW PUMP 03/06/2014
ABIOMED IMPELLA CP 02/18/2014
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