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

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
 

 
 
 1 
 2 
 > 
 
18 records meeting your search criteria returned- Product Code: DRF Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC NAVISTAR¿ ELECTROPHYSIOLOGY CATHETER 03/19/2024
BIOSENSE WEBSTER INC DECANAV ELECTROPHYSIOLOGY CATHETER 01/29/2024
BIOSENSE WEBSTER INC DECANAV ELECTROPHYSIOLOGY CATHETER 10/04/2023
BIOSENSE WEBSTER INC OAE 08/24/2023
BOSTON SCIENTIFIC CORPORATION INTELLAMAP ORION HIGH RESOLUTION MAPPING 08/08/2023
BIOSENSE WEBSTER INC DECANAV ELECTROPHYSIOLOGY CATHETER 06/08/2023
BOSTON SCIENTIFIC CORPORATION INTELLAMAP ORION HIGH RESOLUTION MAPPING 12/06/2022
BIOSENSE WEBSTER INC CRISTA CATH¿ ELECTROPHYSIOLOGY CATHETER 10/24/2022
BIOSENSE WEBSTER INC LASSO® NAV ECO CATHETER 02/10/2022
BIOSENSE WEBSTER INC WEBSTER CS 02/06/2022
-
-