• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: GEI Patient Problem: Atrial Fibrillation 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 12/06/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) PULSAR II GENERATOR 12/06/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) AEX GENERATOR 10/01/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) UNKNOWN MAE DEVICE 10/01/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) UNKNOWN MAE DEVICE 08/10/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) UNKNOWN MAE DEVICE 08/10/2022
PERFUSION SYSTEMS BP2 ABLATION DEVICE BIOPOLAR DEVICE 12/21/2021
MEDTRONIC, INC. BP2 ABLATION DEVICE BIOPOLAR DEVICE 12/21/2021
COVIDIEN LP BARRX BARRX 05/04/2020
COVIDIEN LP BARRX UNKNOWN BARRX 360 05/01/2020
-
-