• 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
 

 
 
10 records meeting your search criteria returned- Product Code: DQO Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CORPORATION UNKNOWN SUPERTORQUE CATHETER 04/01/2022
COOK, INC. COOK MEDICAL RADIAL ARTERY CATHETER SET, 08/17/2021
COOK, INC. COOK MEDICAL RADIAL ARTERY CATHETER SET, 08/17/2021
CORDIS CORPORATION SUPER TORQUE 08/08/2019
ANGIODYNAMICS INC SOFT-VUE HEADHUNTER 1 12/06/2018
UNKNOWN 6" FRENCH SHEATH 12/06/2018
MICROVENTION, INC. HEADWAY DUO MICROCATHETER 10/28/2018
MERIT MEDICAL SYSTEMS, INC. IMPRESS 11/09/2016
GUIDANT PUERTO RICO BV unknown brand name 07/01/2015
GUIDANT PUERTO RICO BV unknown brand name 07/02/2014
-
-