• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: DXC Product Problem: Material Puncture/Hole Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION CATHET 06/11/2021
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION DEVICE 06/07/2021
EDWARDS LIFESCIENCES LLC INTRACLUDE INTRA-AORTIC OCCLUSION CATHET 05/14/2021
EDWARDS LIFESCIENCES INTRA-AORTIC OCCLUSION DEVICE 05/14/2021
EDWARDS LIFESCIENCES LLC INTRAAORTIC OCCLUSION DEVICE 04/02/2021
EDWARDS LIFESCIENCES INTRACLUDE 10/02/2020
TERUMO MEDICAL CORPORATION TR BAND 10/31/2019
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION DEVICE 09/10/2019
EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC OCCLUSION DEVICE 04/18/2019
EDWARDS LIFESCIENCES INTRACLUDE 04/16/2019
-
-