• 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 
 3 
 4 
 5 
 6 
 7 
 > 
 
63 records meeting your search criteria returned- Product Code: GEI Patient Problem: Necrosis Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 03/05/2024
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 03/05/2024
ERBE ELEKTROMEDIZIN GMBH ERBE ICC 200 E/A 02/26/2024
COVIDIEN MFG DC BOULDER EDGE 01/31/2024
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 01/31/2024
ARTHROCARE CORPORATION UNKN ENT REFLEX ULTRA PLASMA WAND AND TU 11/28/2023
ARTHROCARE CORPORATION UNKN ENT REFLEX ULTRA PLASMA WAND AND TU 11/28/2023
SMITH & NEPHEW, INC. UNKNOWN ARTHROSCOPY & TECHNOLOGY DEV 11/16/2023
3M COMPANY VALLEY PLANT 3M¿ UNIVERSAL ELECTROSURGICAL PAD 11/15/2023
COVIDIEN MFG DC BOULDER UNKNOWN COOL-TIP RF ABLATION GENERATOR 08/14/2023
-
-