• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
112 records meeting your search criteria returned- Product Code: DWF Product Problem: Break Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROCARE CORP CLEAR-VIEW ACCESS NEEDLE 11/18/2014
EDWARDS LIFESCIENCES VENT CATHETER 10/28/2014
PERFUSION SYSTEMS FLEXIBLE ARCH ARTERIAL CANNULA 10/20/2014
MAQUET CARDIOPULMONARY AG JVP 38# VENT PLUG 3/8 10/15/2014
BD BD ARTERIAL CANNULA WITH FLOWSWITCH 20G 10/02/2014
MEDTRONIC DLP AORTIC ROOT CANNULAE 09/24/2014
DATASCOPE CORP., BEQ-TOP 48000 09/11/2014
MAQUET CARDIOPULMONARY AG 10031#AVALON ELITE 31F, 31CM 08/08/2014
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 08/06/2014
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 07/02/2014
-
-