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 
 > 
 
27 records meeting your search criteria returned- Product Code: MED Product Problem: Use of Device Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ADVANCED STERILIZATION PRODUCTS CIDEX® OPA SOLUTION 12/06/2021
ADVANCED STERILIZATION PRODUCTS CIDEX® OPA SOLUTION 11/30/2021
ADVANCED STERILIZATION PRODUCTS CIDEX® OPA SOLUTION 11/30/2021
STERIS CORPORATION REVITAL-OX RESERT HIGH LEVEL DISINFECTAN 09/29/2021
STERIS CANADA CORPORATION SYSTEM 1 EXPRESS 12/11/2019
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX® OPA SOLUTION 06/20/2019
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX® OPA SOLUTION 06/20/2019
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX® OPA SOLUTION 06/20/2019
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX® OPA SOLUTION 06/20/2019
ADVANCED STERILIZATION PRODUCTS US CIDEX® OPA SOLUTION 05/31/2018
-
-