• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
109 records meeting your search criteria returned- Product Code: FEB Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDIVATORS DSD-201 04/18/2017
MEDIVATORS DSD EDGE 04/18/2017
MEDIVATORS DSD-201 04/12/2017
MEDIVATORS INTERCEPT DETEGENT 04/04/2017
MEDIVATORS RAPICIDE PA 04/03/2017
MEDIVATORS RAPICIDE PA PART A 03/31/2017
CUSTOM ULTRASONICS INC. SYSTEM 83 PLUS 03/10/2017
MEDIVATORS RAPICIDE PA 01/31/2017
MEDIVATORS INTERCEPT DETERGENT 01/19/2017
MEDIVATORS RAPICIDE PA 09/29/2016
-
-