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 
 > 
 
87 records meeting your search criteria returned- Product Code: GEI Patient Problem: Electric Shock Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. SYNERGYRF¿ CONSOLE 11/16/2021
STRYKER ENDOSCOPY-SAN JOSE SERFAS ENERGY 90-S CRUISE 10/14/2021
CONMED CORPORATION CONMED BOVIE UNIT 09/01/2021
OLYMPUS MEDICAL SYSTEMS CORP. A CORD 07/19/2021
OLYMPUS MEDICAL SYSTEMS CORP. A CORD 07/19/2021
CONSOLIDATED MEDICAL EQUIPMENT HYFRECATOR 2000, 115V 05/19/2021
ARTHROCARE CORP. EVAC 70 XTRA COBLATOR II 05/13/2021
CONMED CORPORATION MEDCON CORP HYFRECATOR 2000 05/06/2021
MEDTRONIC ADVANCED ENERGY (SALIENT) AEX GENERATOR 03/24/2021
MEDTRONIC ADVANCED ENERGY (SALIENT) PLASMABLADE 3.0S 03/24/2021
-
-