• 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 
 5 
 6 
 7 
 8 
 9 
 > 
 
83 records meeting your search criteria returned- Product Code: NIQ Product Problem: Material Split, Cut or Torn Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 05/27/2022
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 11/30/2021
ABBOTT VASCULAR XIENCE ALPINE OTW EVEROLIMUS ELUTING COR 10/11/2021
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 10/04/2021
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 09/17/2021
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 09/17/2021
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 09/14/2021
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 08/23/2021
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 06/28/2021
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 05/17/2021
-
-