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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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68 records meeting your search criteria returned- Product Code: DTQ Product Problem: Device Inoperable Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 07/11/2017
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO ADVANCED PERFUSION SYSTEM 1 06/30/2017
TERUMO CARDIOVASCULAR SYSTEM CORPORATIO ADVANCED PERFUSION SYSTEM 1 06/26/2017
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 06/12/2017
MAQUET CARDIOPULMONARY AG HL-20 INTEGRATED PERFUSION SYSTEM 05/30/2017
TERUMO CARDIOVASCULAR SYSTEM CORPORATION ADVANCED PERFUSION SYSTEM 1 05/19/2017
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 05/09/2017
TERUMO CARDIOVASCULAR SYSTEMS CORP. ADVANCED PERFUSION SYSTEM 1 04/21/2017
TERUMO CARDIOVASCULAR SYSTEMS CORP. ADVANCED PERFUSION SYSTEM 1 04/19/2017
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 03/20/2017
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