Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
86 records meeting your search criteria returned- Product Code: MJN Product Problem: Burst Container or Vessel Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA HYPERFORM LINE EXTENSION 02/18/2019
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 02/13/2019
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA HYPERFORM 11/16/2018
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA HYPERFORM 11/07/2018
COVIDIEN (IRVINE) HYPERGLIDE 07/03/2018
COVIDIEN (IRVINE) HYPERFORM 04/09/2018
COVIDIEN (IRVINE) HYPERFORM 03/07/2018
COVIDIEN (IRVINE) HYPERFORM 03/06/2018
COVIDIEN (IRVINE) HYPERGLIDE 02/13/2018
MICRO THERAPEUTICS, INC. D/B/A EV3 NEURO HYPERFORM 01/23/2018
-
-