• 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 
 > 
 
75 records meeting your search criteria returned- Product Code: GEI Product Problem: Display or Visual Feedback Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 06/29/2020
MEDTRONIC/COVIDIEN LLC LIGASURE MARYLAND JAW LAPAROSCOPIC SEALE 06/19/2020
ARTHROCARE CORP. AMBIENT SUPER TURBOVAC 90 IFS 06/14/2020
ARTHROCARE CORP. AMBIENT HIPVAC 50 IFS 06/14/2020
ARTHROCARE CORP. AMBIENT SUPER TURBOVAC 90 IFS 06/14/2020
ARTHROCARE CORP. QUANTUM 2 CONTROLLER 06/05/2020
ARTHROCARE CORP. AMBIENT SUPER TURBOVAC 90 IFS 06/03/2020
ARTHROCARE CORP. QUANTUM 2 CONTROLLER 05/30/2020
GYRUS ACMI, INC MULTIDEBRIDER POWER CONSOLE 05/27/2020
GYRUS ACMI, INC G400 GENERATOR, GYRUS 05/21/2020
-
-