• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: DWF Patient Problem: Aortic Dissection Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PERFUSION SYSTEMS EOPA ARTERIAL CANNULA 02/27/2020
MEDTRONIC, INC. DLP AORTIC ROOT CANNULA WITH FLOW-GUARD 04/23/2019
EDWARDS LIFESCIENCES HEARTPORT ENDOARTERIAL RETURN CANNULA 05/01/2018
EDWARDS LIFESCIENCES EZ GLIDE AORTIC CANNULA, AORTIC PERFUSIO 05/01/2018
EDWARDS LIFESCIENCES ENDODIRECT ARTERIAL CANNULA 03/10/2017
PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE ANTEGRADE CA 01/13/2017
EDWARDS LIFESCIENCES ENDORETURN ARTERIAL CANNULA 10/04/2016
MEDTRONIC PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE ANTEGRADE CAN 12/23/2015
MEDTRONIC PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE CANNULA W/VEN 12/14/2015
MEDTRONIC DLP 11/25/2015
-
-