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 
 > 
 
35 records meeting your search criteria returned- Product Code: DRO Product Problem: Device Displays Incorrect Message Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN ADULT MULTI-FUNCTION DEFIBRILLATION ELEC 11/15/2018
ZOLL MEDICAL CORPORATION M SERIES 05/22/2018
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/18/2018
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/07/2018
ZOLL MEDICAL CORPORATION X SERIES 12/05/2016
ZOLL MEDICAL CORPORATION E SERIES DEFIBRILLATOR 08/22/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 08/04/2016
ZOLL MEDICAL CORPORATION M SERIES 08/01/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 07/01/2016
ZOLL MEDICAL CORPORATION E SERIES DEFIBRILLATOR 05/18/2016
-
-