• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
120 records meeting your search criteria returned- Product Code: NIP Patient Problem: Insufficient Information Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR SUPERA PERIPHERAL STENT SYSTEM 03/29/2021
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 03/25/2021
ABBOTT VASCULAR SUPERA 03/24/2021
ABBOTT VASCULAR SUPERA SELF EXPANDING PERIPHERAL STENT S 03/24/2021
COVIDIEN EVERFLEX SELF-EXPANDING PERIPHERAL STENT 03/22/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 03/16/2021
ABBOTT VASCULAR INC. SUPERA 03/04/2021
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 03/03/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 03/02/2021
EV3 INC./ MEDTRONIC, INC. PERIPHERAL STENT SYSTEM 03/02/2021
-
-