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 
 3 
 4 
 > 
 
38 records meeting your search criteria returned- Product Code: DWF Patient Problem: Cardiac Perforation Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 08/07/2023
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 02/25/2022
CARDIAC ASSIST, INC. LIFESPARC 02/08/2022
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 12/29/2021
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 02/03/2021
PERFUSION SYSTEMS DLP SILICONE RCSP RETROGRADE RETROGRADE 12/22/2020
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 10/09/2020
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 09/02/2020
CARDIACASSIST, INC. PROTEK DUO VENO-VENOUS CANNULA 12/09/2019
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANULA 08/22/2019
-
-