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
 

 
 
5 records meeting your search criteria returned- Product Code: DWF Patient Problem: Atrial Perforation Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ORIGEN BIOMEDICAL, INC ORIGEN REINFORCED DUAL LUMEN CATHETER 03/13/2019
ORIGEN BIOMEDICAL, INC ORIGEN REINFORNCED DUAL LUMEN CATHETER 03/13/2019
COOK VASCULAR INC VITAL-PORT DETACHED SILICONE CATHETER TI 10/11/2016
MAQUET CARDIOVASCULAR AVALON CLITE 31FR. CANNULA 01/22/2015
EDWARDS LIFESCIENCES PROPLEGE CORONARY SINUS CATHETER 07/11/2014
-
-