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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
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
LAKE REGION MEDICAL THRUWAY GUIDEWIRE 01/08/2019
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 01/04/2019
AV-TEMECULA-CT 0.014 HI-TORQUE (HT) TURNTRAC GUIDE WIRE 12/19/2018
AV-TEMECULA-CT HI-TORQUE FLOPPY II GUIDE WIRE 12/14/2018
MEDTRONIC, INC ZINGER GUIDE WIRE 12/07/2018
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 11/16/2018
COOK INC ROADRUNNER NIMBLE FLOPPY HYDROPHILIC WIR 09/21/2018
COOK INC ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUI 09/19/2018
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 09/11/2018
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 08/23/2018
-
-