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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
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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16 records meeting your search criteria returned- Product Code: DWA Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 02/11/2019
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 11/20/2018
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 11/20/2018
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 09/13/2018
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 08/30/2018
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 08/11/2018
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 08/10/2018
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR 07/26/2018
THORATEC SWITZERLAND GMBH THORATEC CENTRIMAG PRIMARY CONSOLE 05/14/2018
THORATEC SWITZERLAND GMBH THORATEC CENTRIMAG PRIMARY CONSOLE 04/06/2018
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