• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: DQX Product Problem: Material Distortion Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC, INC ZINGER GUIDE WIRE 01/15/2018
VOLCANO CORPORATION VERRATA PRESSURE GUIDE WIRE 12/28/2017
ARROW ARROW QUICKFLASH RADIAL ARTERY CATHETER 12/18/2017
MEDTRONIC, INC COUGAR GUIDE WIRE 06/28/2017
MEDTRONIC, INC COUGAR GUIDE WIRE 06/15/2017
LAKE REGION MEDICAL PREFORM GUIDEWIRE - SAFARI2 03/07/2017
LAKE REGION MEDICAL PREFORM GUIDEWIRE - SAFARI2 03/07/2017
LAKE REGION MEDICAL PREFORM GUIDEWIRE - SAFARI2 11/02/2016
LAKE REGION MEDICAL PREFORM GUIDEWIRE - SAFARI2 11/02/2016
VOLCANO CORPORATION VERRATA PRESSURE GUIDE WIRE 05/11/2016
-
-