• 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 
 > 
 
25 records meeting your search criteria returned- Product Code: DWF Product Problem: Material Twisted/Bent Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH CANNULA & CATHETER 08/07/2023
LIVANOVA USA INC CARIOP CANN + VENT 14 GA 05/09/2023
PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE ANTEGRADE CA 04/13/2023
PERFUSION SYSTEMS MC2 TWO STAGE VENOUS CANNULA 03/29/2023
PERFUSION SYSTEMS MC2 TWO STAGE VENOUS CANNULA 03/29/2023
MEDTRONIC MEXICO BIO-MEDICUS NG PEDIATRIC ARTERIAL CANNUL 03/08/2023
PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE ANTEGRADE CANN 03/07/2023
PERFUSION SYSTEMS BIOMEDICUS MULTISTAGE FEMORAL VENOUS CAN 02/28/2023
MAQUET CARDIOPULMONARY GMBH CANNULA & CATHETER 12/05/2022
MAQUET CARDIOPULMONARY GMBH CANNULA & CATHETER 12/05/2022
-
-