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
 

 
 
8 records meeting your search criteria returned- Product Code: FDA Product Problem: Device Reprocessing Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AIZU OLYMPUS CO., LTD. EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE 09/12/2023
AIZU OLYMPUS CO., LTD. EVIS LUCERA ELITE SMALL INTESTINAL VIDEO 08/31/2023
AIZU OLYMPUS CO., LTD. EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE 08/31/2023
AIZU OLYMPUS CO., LTD. EVIS EXERA II SMALL INTESTINAL VIDEOSCOP 06/14/2023
AIZU OLYMPUS CO., LTD. EVIS LUCERA ELITE SMALL INTESTINAL VIDEO 04/19/2023
AIZU OLYMPUS CO., LTD. EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE 12/14/2022
FUJIFILM TECHNO PRODUCTS, MITO FACTORY FUJINON 06/08/2017
FUJIFILM TECHNO PRODUCTS CO., LTD. MITO FUJIFILM 07/13/2016
-
-