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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC ADVANCED ENERGY (SALIENT) UNKNOWN MAE DEVICE 06/28/2021
MEDTRONIC ADVANCED ENERGY (SALIENT) AEX GENERATOR-REFURB 06/28/2021
OLYMPUS WINTER & IBE GMBH CELONLAB ENT 100-120 V~ (KIT) 11/18/2020
OLYMPUS WINTER & IBE GMBH CELONLAB ENT 100-120 V~ (KIT) 11/16/2020
COVIDIEN MEDICAL PRODUCTS FORCE FX 08/20/2020
ARTHREX, INC. APOLLORF XL90, ASPIRATING ABLATOR 90° 11/22/2019
MEGADYNE MEDICAL PRODUCTS, INC. UNK_PATIENT RETURN ELECTRODES - REUSABLE 10/08/2019
OLYMPUS MEDICAL SYSTEMS CORP. ELECTROSURGICAL UNIT 07/30/2019
CONMED ELECTROSURGERY SYSTEM 5000 07/26/2019
CONMED ELECTROSURGERY SYSTEM 5000 07/26/2019
-
-