• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 > 
 
37 records meeting your search criteria returned- Product Code: DSY Patient Problem: Insufficient Information Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOVASCULAR LLC UNKNOWN 09/08/2023
ATRIUM MEDICAL CORPORATION FLIXENE GRAFTS W/GDS 08/29/2023
W. L. GORE & ASSOCIATES, INC. GORE-TEX® STRETCH VASCULAR GRAFT 08/27/2023
VASCUTEK LTD GELWEAVE VALSALVA 08/08/2023
VASCUTEK LTD Gelweave¿ 06/29/2023
W. L. GORE & ASSOCIATES, INC. GORE® ACUSEAL VASCULAR GRAFT 12/06/2022
W. L. GORE & ASSOCIATES, INC. GORE® ACUSEAL VASCULAR GRAFT 12/06/2022
VASCUTEK LTD. GELWEAVE 11/04/2022
VASCUTEK LTD. GELSOFT PLUS 09/29/2022
VASCUTEK LTD. GELWEAVE 09/16/2022
-
-