• 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 
 3 
 4 
 > 
 
40 records meeting your search criteria returned- Product Code: MHY Product Problem: Device Or Device Fragments Location Unknown Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/02/2018
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 06/27/2018
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE ELECTRICAL LEAD 06/27/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 06/18/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 06/14/2018
MEDTRONIC MED REL MEDTRONIC PUERTO RICO SOLETRA 06/05/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 06/01/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 05/15/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 04/26/2018
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 04/26/2018
-
-