• 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 
 10 
 > 
 
123 records meeting your search criteria returned- Product Code: GEI Product Problem: Noise, Audible Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN MFG DC BOULDER LIGASURE 10/07/2022
OLYMPUS WINTER & IBE GMBH HF UNIT "ESG-400" 09/28/2022
COVIDIEN LP LIGASURE 09/13/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) AEX GENERATOR 09/01/2022
OLYMPUS WINTER & IBE GMBH ELECTROSURGICAL GENERATOR "ESG-400" 08/31/2022
ETHICON ENDO-SURGERY, LLC. ENSEAL G2 CURVED JAW 35CM 08/18/2022
KARL STORZ SE & CO. KG STORZ BIPOLAR BOVIE 07/29/2022
SOLTA MEDICAL INC THERMAGE CPT SYSTEM TIP 07/07/2022
COVIDIEN MFG DC BOULDER LIGASURE 07/01/2022
OLYMPUS MEDICAL SYSTEMS CORP. ELECTROSURGICAL UNIT 06/24/2022
-
-