• 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 
 > 
 
17 records meeting your search criteria returned- Product Code: DWF Patient Problem: Thrombosis/Thrombus Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES LLC RETROGRADE CORONARY SINUS CANNULA 08/12/2023
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 08/07/2023
PERFUSION SYSTEMS BIO-MEDICUS NG 21 FR VENOUS CANNULA 02/03/2023
PERFUSION SYSTEMS BIO-MEDICUS NG PEDIATRIC ARTERIAL CANNUL 12/02/2022
PERFUSION SYSTEMS BIO-MEDICUS NG 25 FR VENOUS CANNULA 12/02/2022
PERFUSION SYSTEMS BIO-MEDICUS NG 15 FR VENOUS CANNULA 12/02/2022
PERFUSION SYSTEMS BIO-MEDICUS NG PEDIATRIC ARTERIAL CANNUL 12/02/2022
PERFUSION SYSTEMS PEDIATRIC BIOMEDICUS FEMORAL CANNULA 12/02/2022
PERFUSION SYSTEMS BIO-MEDICUS NG 23 FR VENOUS CANNULA 11/18/2022
PERFUSION SYSTEMS CANNULA 96530-123 BIO-MEDICUS 23FR EA 11/11/2022
-
-