• 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 
 > 
 
18 records meeting your search criteria returned- Product Code: FDT Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE MODEL ED-580XT 08/31/2023
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE ED-580XT 06/20/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE MODEL ED-580XT 04/27/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE MODEL ED-580XT 04/27/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE MODEL ED-580XT 04/21/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE MODEL ED-580XT 04/21/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE ED-580XT 04/19/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE ED-580XT 01/10/2022
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE ED-580XT 12/22/2021
FUJIFILM CORPORATION FUJIFILM DUODENOSCOPE ED-580XT 12/15/2021
-
-