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

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 
 > 
 
145 records meeting your search criteria returned- Product Code: GEI Product Problem: Failure to Power Up Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ENDOSCOPY-SAN JOSE PKG, CROSSFIRE 2 CONSOLE 05/25/2023
STRYKER ENDOSCOPY-SAN JOSE PKG, CROSSFIRE 2 CONSOLE 05/02/2023
SHIRAKAWA OLYMPUS CO., LTD. ELECTROSURGICAL UNIT 03/15/2023
ARTHROCARE CORPORATION COBLATOR II CONTROLLER (240V) 12/16/2022
STRYKER ENDOSCOPY-SAN JOSE SERFAS ENERGY 90-S CRUISE 10/17/2022
STRYKER ENDOSCOPY-SAN JOSE SERFAS ENERGY 90-S CRUISE 10/17/2022
STRYKER ENDOSCOPY-SAN JOSE SERFAS ENERGY 90-S CRUISE 10/17/2022
MEDTRONIC, INC. LIGHTED RESTRACTOR SOLSTICE B1 10/01/2022
MEDTRONIC, INC. LIGHTED RESTRACTOR SOLSTICE B1 10/01/2022
ARTHROCARE CORP. COBLATOR II CONTROLLER (240V) 02/28/2022
-
-