• 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
 

 
 
8 records meeting your search criteria returned- Product Code: DWF Product Problem: Device Operational Issue Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA DEUTSCHLAND ELECTRICAL VENOUS OCCLUDER (EVO) 01/16/2018
LIVANOVA DEUTSCHLAND ELECTRICAL VENOUS OCCLUDER (EVO) 12/20/2017
MC3, INCORPORATED MC3 SOFT-FLOW AORTIC CANNULA 12/12/2017
MC3, INCORPORATED MC3 SOFT-FLOW AORTIC CANNULA 12/12/2017
MC3, INCORPORATED MC3 SOFT-FLOW AORTIC CANNULA 12/12/2017
LIVANOVA DEUTSCHLAND ELECTICAL VENOUS OCCLUDER (EVO) 10/24/2017
LIVANOVA DEUTSCHLAND ELECTRICAL VENOUS OCCLUDER (EVO) 09/08/2017
LIVANOVA DEUTSCHLAND ELECTICAL VENOUS OCCLUDER (EVO) 05/19/2017
-
-