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
 

 
 < 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 19 
 > 
 
183 records meeting your search criteria returned- Product Code: EZW Product Problem: Human-Device Interface Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION INTERSTIM II 04/07/2016
MEDTRONIC NEUROMODULATION INTERSTIM 02/12/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM II 02/09/2016
MPRI INTERSTIM 02/05/2016
MEDTRONIC MED REL MEDTRONIC PUERTO RICO INTERSTIM II 01/29/2016
MEDTRONIC NEUROMODULATION UNKNOWN INTERSTIM LEAD 12/17/2015
MEDTRONIC NEUROMODULATION UNKNOWN INTERSTIM LEAD 12/17/2015
NEURO - VILLALBA INTERSTIM 12/14/2015
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM II 09/18/2015
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM II 08/10/2015
-
-