• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 
 
19 records meeting your search criteria returned- Product Code: MRU Product Problem: Therapy Delivered to Incorrect Body Area Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/02/2016
MEDTRONIC NEUROMODULATION SOLETRA 07/07/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 01/26/2016
IPG MFG SWITZERLAND ACTIVA 12/16/2015
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 08/31/2015
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 05/27/2015
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 02/17/2015
IPG MFG SWITZERLAND ACTIVA 09/10/2014
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 03/27/2014
-
-