• 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
132 records meeting your search criteria returned- Product Code: DWF Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PERFUSION SYSTEMS ARTERIAL CANNULA 02/22/2024
PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE ANTEGRADE CA 01/22/2024
PERFUSION SYSTEMS EOPA ARTERIAL CANNULA 01/16/2024
PERFUSION SYSTEMS EOPA ARTERIAL CANNULA 01/16/2024
PERFUSION SYSTEMS EOPA ARTERIAL CANNULA 01/16/2024
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 12/08/2023
PERFUSION SYSTEMS DLP CURVED TIP ARTERIAL CANNULA 11/20/2023
THORATEC SWITZERLAND GMBH CENTRIMAG 34F DRAINAGE (VENOUS) CANNULA 10/25/2023
THORATEC SWITZERLAND GMBH CENTRIMAG TUBING PACK 09/29/2023
MEDTRONIC MEXICO BIO-MEDICUS NG PEDIATRIC ARTERIAL CANNUL 09/29/2023
-
-