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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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135 records meeting your search criteria returned- Product Code: DSQ Product Problem: Device Inoperable Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
HEARTWARE HEARTWARE HVAD 09/19/2016
THORATEC THORATEC HEARTMATE II 08/05/2016
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM 03/03/2016
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM 03/03/2016
THORATEC HEARTMATEII LVAD 02/19/2016
THORATEC CORPORATION HEARTMATE II 01/12/2016
MAQUET CARDIOVASCULAR, LLC ROTAFLOW PUMP 10/31/2015
THORATEC CORPORATION HEARTMATE II LEFT VENTRICULAR ASSIST DEV 09/30/2015
HEARTWARE, INC HEARTWARE® VENTRICULAR ASSIST SYSTEM 06/01/2015
THORATEC CORPORATION HEARTMATE II LVAD 05/04/2015
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