• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
141 records meeting your search criteria returned- Product Code: NIU Patient Problem: Obstruction/Occlusion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOK IRELAND LTD ZILVER PTX DRUG-ELUTING PERIPHERAL STENT 12/19/2022
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 12/19/2022
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 12/19/2022
BOSTON SCIENTIFIC CORPORATION ELUVIA DRUG-ELUTING VASCULAR STENT SYSTE 12/08/2022
BOSTON SCIENTIFIC CORPORATION ELUVIA DRUG-ELUTING VASCULAR STENT SYSTE 12/08/2022
BOSTON SCIENTIFIC CORPORATION ELUVIA DRUG-ELUTING VASCULAR STENT SYSTE 11/16/2022
COOK IRELAND LTD ZILVER PACLITAXEL-ELUTING PERIPHERAL STE 11/15/2022
BOSTON SCIENTIFIC CORPORATION ELUVIA DRUG-ELUTING VASCULAR STENT SYSTE 10/31/2022
BOSTON SCIENTIFIC CORPORATION ELUVIA DRUG-ELUTING VASCULAR STENT SYSTE 09/16/2022
BOSTON SCIENTIFIC CORPORATION ELUVIATM DRUG-ELUTING VASCULAR STENT SYS 09/13/2022
-
-