• 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 
 > 
 
50 records meeting your search criteria returned- Product Code: DWF Product Problem: Nonstandard Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES EDWARDS MANUALLY INFLATING RETROGRADE CA 10/28/2022
EDWARDS LIFESCIENCES EDWARDS LIFESCIENCES EZ GLIDE AORTIC CAN 07/13/2022
EDWARDS LIFESCIENCES EDWARDS LIFESCIENCES EZ GLIDE AORTIC CAN 07/08/2022
EDWARDS LIFESCIENCES EZ GLIDE AORTIC CANNULA 07/08/2022
EDWARDS LIFESCIENCES EDWARDS ENDORETURN ARTERIAL CANNULA 04/22/2022
MEDTRONIC MEDTRONIC PERFUSION CUSTOM TUBING PACKS 12/16/2021
BARD PERIPHERAL VASCULAR, INC. JAVID SHUNT 03/15/2021
MEDTRONIC MEXICO S. DE R.L. DE CV CUSTOM TUBING PACK 03/03/2021
EDWARDS LIFESCIENCES EZ GLIDE AORTIC CANNULA, AORTIC PERFUSIO 03/13/2020
EDWARDS LIFESCIENCES EZ GLIDE AORTIC CANNULA 02/01/2020
-
-