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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
113 records meeting your search criteria returned- Product Code: LWR Patient Problem: Congestive Heart Failure Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES EDWARDS INSPIRIS RESILIA AORTIC VALVE 01/11/2021
ST. JUDE MEDICAL, COSTA RICA LTDA (SH) TRIFECTA STENTED TISSUE VALVE 12/01/2020
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 11/26/2020
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 11/26/2020
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) SJM TRIFECTA VALVE 11/25/2020
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) TRIFECTA GT VALVE 10/21/2020
ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA SJM TRIFECTA VALVE 10/05/2020
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) TRIFECTA GT VALVE 09/15/2020
EDWARDS LIFESCIENCES EDWARDS INSPIRIS RESILIA AORTIC VALVE 09/01/2020
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 07/25/2020
-
-