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 
 > 
 
33 records meeting your search criteria returned- Product Code: DWF Patient Problem: No Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES RETROGRADE CANNULAE 07/16/2018
SURGE CARDIOVASCULAR SURGE CARDIOVASCULAR RETROGRADE MANUAL I 07/05/2018
MAQUET CARDIOPULMONARY AG 10031#AVALON ELITE 31F 07/02/2018
MAQUET CARDIOPULMONARY AG CATHETER, CANNULA AND TUBING, VASCULAR, 07/02/2018
SURGE CARDIOVASCULAR ANTEGRADE CARDIOPLEGIA CANNULA 05/15/2018
MAQUET CARDIOPULMONARY AG CATHETER,CANNULA AND TUBING,VASCULAR 04/16/2018
MEDTRONIC, INC. AORTIC ROOT CANNULA 01/04/2018
EDWARDS LIFESCIENCES QUICKDRAW VENOUS CANNULAE 12/20/2017
ORIGEN BIOMEDICAL ORIGEN VV 19FR CANNULA 12/04/2017
EDWARDS LIFESCIENCES ENDOVENT 10/20/2017
-
-