• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: FDS Product Problem: Residue After Decontamination Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 10/25/2023
AIZU OLYMPUS CO., LTD. EVIS EXERA III GASTROINTESTINAL VIDEOSCO 07/31/2023
AIZU OLYMPUS CO., LTD. GASTROINTESTINAL VIDEOSCOPE 07/31/2023
AIZU OLYMPUS CO., LTD. AUXILIARY WATER TUBE 07/17/2023
AIZU OLYMPUS CO., LTD. AUXILIARY WATER TUBE 07/17/2023
AIZU OLYMPUS CO., LTD. AUXILIARY WATER TUBE 07/17/2023
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA III GASTROINTESTINAL VIDEOSCO 01/05/2022
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 12/02/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA II GASTROINTESTINAL VIDEOSCOP 11/29/2021
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 11/23/2021
-
-