• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
197 records meeting your search criteria returned- Product Code: DQX Product Problem: Device Damaged by Another Device Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONFLUENT MEDICAL TECHNOLOGIES AQUATRACK HYDROPHILIC NITINOL GUIDEWIRE 05/06/2019
MEDTRONIC, INC COUGAR GUIDE WIRE 04/04/2019
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 03/15/2019
AV-TEMECULA-CT HT VERSATURN GUIDE WIRE 02/28/2019
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 02/25/2019
AV-TEMECULA-CT ACS HI-TORQUE IRON MAN GUIDE WIRE 02/25/2019
AV-TEMECULA-CT ACS HI-TORQUE EXTRA SPORT GUIDE WIRE WI 02/22/2019
AV-TEMECULA-CT HI-TORQUE WHISPER MS GUIDE WIRE 02/14/2019
LAKE REGION MEDICAL THRUWAY GUIDEWIRE 02/06/2019
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 01/24/2019
-
-