• 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
 

 
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
 
204 records meeting your search criteria returned- Product Code: NIP Product Problem: Difficult to Advance Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 09/29/2020
ABBOTT VASCULAR ABSOLUTE PRO LL SELF-EXPANDING STENT SYS 09/24/2020
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 09/23/2020
ABBOTT VASCULAR SUPERA PERIPHERAL STENT SYSTEM 09/17/2020
COVIDIEN EVERFLEX SELF-EXPANDING PERIPHERAL STENT 09/08/2020
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 09/06/2020
BOSTON SCIENTIFIC CORPORATION INNOVA VASCULAR 09/04/2020
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 08/28/2020
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 08/17/2020
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT STENT SYSTEM 07/14/2020
-
-