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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
154 records meeting your search criteria returned- Product Code: DXC Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CV HS III PROXIMAL SEAL SYTEM 4.3MM 12/20/2016
MAQUET CV AXIUS CORONARY SHUNT 1.0 MM 12/16/2016
TELEFLEX MEDICAL SATINSKY CLAMP SMALL AG 12/06/2016
TELEFLEX MEDICAL (PILLING-WECK SUBSIDIAR PILLING SATINSKY CLAMP 11/28/2016
TERUMO CORPORATION, ASHITAKA TR BAND 10/26/2016
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION DEVICE 10/10/2016
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION DEVICE 10/04/2016
TERUMO MEDICAL CORP. TR BAND 09/02/2016
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION DEVICE 08/01/2016
ST. JUDE MEDICAL, INC. ANGIOSEAL 6 FR 06/29/2016
-
-