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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
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
ABBOTT VASCULAR HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL 03/12/2024
ABBOTT VASCULAR HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE WIR 03/11/2024
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 01/11/2024
ABBOTT VASCULAR HI-TORQUE TURNTRAC GUIDE WIRE 12/13/2023
ABBOTT VASCULAR HI-TORQUE TURNTRAC GUIDE WIRES 12/12/2023
ABBOTT VASCULAR HT VERSATURN GUIDE WIRE 12/05/2023
MEDTRONIC, INC COUGAR GUIDE WIRE 11/21/2023
ABBOTT VASCULAR HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL 11/09/2023
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 09/12/2023
LAKE REGION MEDICAL ZIPWIRE HYDROPHILIC GUIDEWIRE 07/19/2023
-
-