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 
 
 
11 records meeting your search criteria returned- Product Code: DWF Product Problem: Defective Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GETINGE AB/ MAQUET CARDIOPULMONARY GMBH MAQUET VENOUS HLS CANNULA 06/09/2023
MEDTRONIC, INC. MEDTRONIC BIO-MEDICUS FEMORAL ARTERY CAN 06/02/2023
ANGIODYNAMICS, INC ANGIOVAC CANNULA 12/10/2021
MAQUET CARDIOPULMONARY GMBH CATHETER, CANNULA AND TUBING, VASCULAR, 11/03/2020
EDWARDS LIFESCIENCES EDWARDS LIFESCIENCES AVID DUAL STAGE VEN 06/30/2020
ANGIODYNAMICS, INC. ANGIODYNAMICS / ANGIOVAC 09/26/2019
ORIGEN BIOMEDICAL, INC ORIGEN REINFORCED DUAL LUMEN CATHETER 04/02/2019
EDWARDS LIFESCIENCES RETROGRADE CARDIOPLEGIA CATHETER BALLOON 10/17/2018
MEDTRONIC, INC. AORTIC ROOT CANNULA 01/04/2018
DATASCOPE CORP. CUSTOM TUBING PACK 03/24/2015
-
-