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 
 > 
 
39 records meeting your search criteria returned- Product Code: FAJ Product Problem: Device Reprocessing Problem Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. FIBERSCOPE "CYF-5", EUROPEAN VERSION 07/10/2020
OLYMPUS MEDICAL SYSTEMS CORP. FIBERSCOPE "CYF-5", EUROPEAN VERSION 07/10/2020
OLYMPUS MEDICAL SYSTEMS CORP. FIBERSCOPE "CYF-5", EUROPEAN VERSION 07/10/2020
OLYMPUS MEDICAL SYSTEMS CORP. VIDEOSCOPE "CYF-V2", EUROPEAN VERSION 06/18/2020
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 06/15/2020
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 04/15/2020
OLYMPUS MEDICAL SYSTEMS CORP. OES CYSTONEPHROFIBERSCOPE 09/16/2019
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 06/23/2017
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 03/14/2016
OLYMPUS MEDICAL SYSTEM CORPORATION FLEXIBLE CYSTONEPHROFIBERSCOPE 02/29/2016
-
-