Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 3 
 > 
 
24 records meeting your search criteria returned- Product Code: DWA Patient Problem: Insufficient Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 10/06/2023
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 06/02/2023
THORATEC CORP. CENTRIMAG 2ND GEN 02/17/2023
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP 5 01/26/2023
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP 5 01/26/2023
THORATEC SWITZERLAND GMBH CENTRIMAG 1ST GENERATION PRIMARY CONSOLE 11/28/2022
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO SARNS CENTRIFUGAL SYSTEM 11/11/2022
THORATEC SWITZERLAND GMBH CENTRIMAG 1ST GENERATION PRIMARY CONSOLE 11/08/2022
PERFUSION SYSTEMS BIO CONSOLE 560 08/16/2022
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 08/03/2022
-
-