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 
 > 
 
38 records meeting your search criteria returned- Product Code: DWF Patient Problem: No Code Available Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES RETROGRADE CANNULAE 08/24/2020
COOK VANDERGRIFT INC VITAL-PORT DETACHED SILICONE CATHETER TI 12/11/2019
PERFUSION SYSTEMS CANNULA CB57517 FEMORAL ART 17FR CARMEDA 07/05/2019
ORIGEN BIOMEDICAL, INC ORIGEN REINFORCED DUAL LUMEN CATHETER 04/02/2019
ORIGEN BIOMEDICAL, INC. ORIGEN REINFORCED DUAL LUMEN CATHETER 03/13/2019
EDWARDS LIFESCIENCES RETROGRADE CORONARY SINUS CARDIOPLEGIA C 10/15/2018
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 05/21/2018
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 05/16/2018
COOK VASCULAR INC VITAL-PORT DETACHED SILICONE CATHETER TI 04/26/2018
EDWARDS LIFESCIENCES SELF-INFLATING RETROGRADE CARDIOPLEGIA C 03/19/2018
-
-