• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
381 records meeting your search criteria returned- Product Code: NIQ Product Problem: Material Rupture Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 07/22/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 07/22/2021
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 07/21/2021
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 07/20/2021
BIOTRONIK AG, BUELACH, SWITZERLAND ORSIRO 2.25/22 07/07/2021
ABBOTT VASCULAR XIENCE PRIME EVEROLIMUS ELUTING CORONARY 06/29/2021
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 06/28/2021
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 06/14/2021
ABBOTT VASCULAR XIENCE XPEDITION 48 EVEROLIMUS ELUTING C 06/14/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 06/07/2021
-
-