• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: MED Patient Problem: Skin Irritation Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX OPA SOLUTION 11/04/2020
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX OPA SOLUTION 11/04/2020
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX OPA SOLUTION 11/04/2020
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX OPA SOLUTION 11/04/2020
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX OPA SOLUTION 11/04/2020
ADVANCED STERILIZATION PRODUCTS DISOPA SOLUTION 08/21/2019
ADVANCED STERILIZATION PRODUCTS EMEA CIDEX® OPA SOLUTION 10/03/2018
STERIS CORPORATION REVITAL-OX RESERT 04/13/2017
ADVANCED STERILIZATION PRODUCTS CIDEX OPA SOLUTION 02/21/2017
STERIS CANADA CORPORATION STERIS SYSTEM 1E 03/29/2016
-
-