• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
100 records meeting your search criteria returned- Product Code: DQY Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND ATTAIN COMMAND 10/06/2016
BOSTON SCIENTIFIC - MAPLE GROVE MACH1 GUIDE CATHETER 10/03/2016
BOSTON SCIENTIFIC - MAPLE GROVE RUNWAY GUIDE CATHETER 08/10/2016
CORDIS CORPORATION VISTA BRITE TIP GUIDING CATHETERS 06/24/2016
BARD PERIPHERAL VASCULAR, INC. RIVAL PTA BALLOON DILATATION CATHETER 04/13/2016
COVIDIEN EVERCROSS 035 01/28/2016
BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE 014 PTA BALLOON DILATATION CA 01/12/2016
BARD PERIPHERAL VASCULAR, INC. VACCESS PTA BALLOON DILATATION CATHETER 01/12/2016
BOSTON SCIENTIFIC - MAPLE GROVE RUBICON¿ 18 12/08/2015
CORDIS CORPORATION 9F/.098" LARGE LUMEN GUIDING CATHETER 10/19/2015
-
-