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

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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
111 records meeting your search criteria returned- Product Code: GEX Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ANGIODYNAMICS PVAK - 400 MICRON FIBER PROCEDURE KIT 08/16/2017
ANGIODYNAMICS PVAK - 400 MICRON FIBER PROCEDURE KIT 08/16/2017
C.R. BARD, INC. (COVINGTON) -1018233 ENDOBEAM¿ HOLMIUM LASER FIBER 07/25/2017
ANGIODYNAMICS EVLT KIT WITH SPOTLIGHT OPS SHEATH 06/27/2017
ANGIODYNAMICS VENCURE NEVERTOUCH 06/07/2017
COOK INC COOK® SINGLE-USE HOLMIUM LASER FIBER 06/01/2017
ANGIODYNAMICS PVAK - 400 MICRON FIBER PROCEDURE KIT 05/17/2017
ANGIODYNAMICS VENCURE NEVERTOUCH 05/17/2017
ANGIODYNAMICS, INC. PVAK - 400 MICRON FIBER PROCEDURE KIT 03/07/2017
ANGIODYNAMICS, INC. VENCURE NEVERTOUCH 03/07/2017
-
-