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 
 > 
 
24 records meeting your search criteria returned- Product Code: NIU Patient Problem: Insufficient Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 02/23/2024
COOK IRELAND LTD ZILVER PTX DRUG-ELUTING PERIPHERAL STENT 10/27/2023
COOK IRELAND LTD ZILVER PACLITAXEL-ELUTING PERIPHERAL STE 08/09/2023
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 06/26/2023
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 06/26/2023
COOK IRELAND LTD ZILVER PTX DRUG-ELUTING PERIPHERAL STENT 06/26/2023
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 06/23/2023
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 06/20/2023
COOK IRELAND LTD ZILVER PTX DRUG-ELUTING PERIPHERAL STENT 12/20/2022
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 12/19/2022
-
-