• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
220 records meeting your search criteria returned- Product Code: DRF Product Problem: Entrapment of Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC LASSO¿ ELECTROPHYSIOLOGY CATHETER 09/01/2021
BIOSENSE WEBSTER INC LASSO NAV ECO VARIABLE CATHETER 08/29/2021
MEDTRONIC MEXICO S. DE R.L. DE CV ACHIEVE MAPPING CATHETER - 20 MM 08/20/2021
ST. JUDE MEDICAL ADVISOR HD GRID MAPPING CATHETER, SENSOR 08/10/2021
BIOSENSE WEBSTER INC LASSO NAV ECO VARIABLE CATHETER 08/03/2021
BIOSENSE WEBSTER INC UNK_LASSO 07/13/2021
BIOSENSE WEBSTER INC UNK_LASSO 07/13/2021
ST. JUDE MEDICAL ADVISOR HD GRID MAPPING CATHETER, SENSOR 07/09/2021
ST. JUDE MEDICAL ADVISOR HD GRID MAPPING CATHETER, SENSOR 06/11/2021
BIOSENSE WEBSTER INC LASSO NAV ECO VARIABLE CATHETER 05/26/2021
-
-