• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
207 records meeting your search criteria returned- Product Code: GEI Product Problem: Therapeutic or Diagnostic Output Failure Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. THUNDERBEAT 02/08/2021
COVIDIEN LP LIGASURE RETRACTABLE L-HOOK LAPAROSCOPIC 02/04/2021
ARTHREX, INC. APOLLO RF 90 MULTIPORT 02/03/2021
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 01/25/2021
ETHICON ENDO-SURGERY, LLC ENSEAL 01/15/2021
CONMED CORPORATION ARGON-ENH (SYSTEM 7500) 01/08/2021
MEDTRONIC NAVIGATION, INC. PLASMABLADE 12/30/2020
ETHICON ENDO-SURGERY, INC. ENSEAL TISSUE SEALER, REF # NSLG2C14 12/16/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO VIRTUOSAPH PLUS WITH RADIAL INDICATION 11/30/2020
MAQUET CARDIOVASCULAR LLC MAQUET VASOVIEW FOR ENDOSCOPIC VEIN HARV 11/25/2020
-
-