• 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 
 > 
 
22 records meeting your search criteria returned- Product Code: NIQ Patient Problem: Failure of Implant Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOTRONIK AG, BUELACH, SWITZERLAND PULSAR-18 6/60/135 04/01/2022
BIOTRONIK AG, BUELACH, SWITZERLAND ORSIRO 2.75/15 08/26/2021
BIOTRONIK AG, BUELACH, SWITZERLAND ORSIRO 3.5/40 04/08/2021
BIOTRONIK AG, BUELACH, SWITZERLAND SYNSIRO 2.5/18 03/15/2021
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 02/16/2021
MEDTRONIC / MEDTRONIC IRELAND RESOLUTE ONYX CORONARY STENT SYSTEM 02/12/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY 09/20/2019
BIOTRONIK AG STENT 07/10/2019
BIOTRONIK AG STENT 07/10/2019
MEDTRONIC IRELAND ENDEAVOR SPRINT RX 08/07/2018
-
-