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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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11 records meeting your search criteria returned- Product Code: KFM Product Problem: Low Battery Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 07/24/2015
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 02/17/2015
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 12/01/2014
TERUMO CARDIOVASCULAR SYSTEMS CORP. TERUMO CENTRIFUGAL SYSTEM 11/26/2014
TERUMO CARDIOVASCULAR SYSTEMS CORP. TERUMO CENTRIFUGAL SYSTEM 11/25/2014
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 10/22/2014
MAQUET CARDIOPULMONARY AG MAQUET CARDIOPULMONARY AG 04/04/2014
MAQUET CARDIOPULMONARY AG MAQUET CARDIOPULMONARY AG 04/03/2014
TERUMO CARDIOVASCULAR SYSTEM CORP TERUMO CENTRIFUGAL SYSTEM 03/27/2014
MAQUET CARDIOPULMONARY AG ROTAFLOW 01/06/2014
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