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 
 3 
 4 
 5 
 > 
 
41 records meeting your search criteria returned- Product Code: DRF Product Problem: Activation, Positioning or Separation Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC. INQUIRY AFOCUSII¿ (4 F DOUBLE LOOP) CATH 03/28/2022
BOSTON SCIENTIFIC CORPORATION INTELLAMAP ORION HIGH RESOLUTION MAPPING 11/17/2021
ST. JUDE MEDICAL INQUIRY STEERABLE DIAGNOSTIC CATHETER 10/15/2021
ST. JUDE MEDICAL INQUIRY STEERABLE DIAGNOSTIC CATHETER 10/15/2021
ST. JUDE MEDICAL, INC. INQUIRY STEERABLE DIAGNOSTIC CATHETER 09/09/2021
ST. JUDE MEDICAL, INC. INQUIRY¿ FIXED CURVE DIAGNOSTIC CATHETER 08/31/2021
BOSTON SCIENTIFIC CORPORATION INTELLAMAP ORION HIGH RESOLUTION MAPPING 07/29/2021
BOSTON SCIENTIFIC CORPORATION INTELLAMAP ORION HIGH RESOLUTION MAPPING 07/09/2021
ST. JUDE MEDICAL INQUIRY STEERABLE DIAGNOSTIC CATHETER 05/20/2021
BOSTON SCIENTIFIC CORPORATION INTELLAMAP ORION HIGH RESOLUTION MAPPING 04/28/2021
-
-