Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
33 records meeting your search criteria returned- Product Code: GEI Patient Problem: Stenosis Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SHIRAKAWA OLYMPUS CO., LTD. OLYMPUS ESG-100, 100...120 V~, 02/21/2024
COVIDIEN MEDICAL PRODUCTS LIGASURE 10/17/2023
COVIDIEN LP BARRX UNKNOWN BARRX 09/15/2023
COVIDIEN LP BARRX UNKNOWN BARRX 09/15/2023
COVIDIEN LP BARRX UNKNOWN BARRX 360 07/11/2023
COVIDIEN LP BARRX UNKNOWN HALO 360 07/11/2023
COVIDIEN LP BARRX UNKNOWN BARRX 07/11/2023
AOMORI OLYMPUS CO., LTD. THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED 06/22/2023
ARTHROCARE CORPORATION UNKNOWN COBLATOR II SURGERY SYSTEM AND W 04/18/2023
COVIDIEN MEDICAL PRODUCTS UNKNOWN EMPRINT ANTENNA 03/23/2023
-
-