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 
 
 
19 records meeting your search criteria returned- Product Code: DRT Product Problem: Device Alarm System Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ZM-531PA 04/05/2017
NIHON KOHDEN CORPORATION ZM-540PA 02/21/2017
WELCH ALLYN PROPAQ ENCORE 206/EL 09/09/2015
GE MEDICAL SYSTEMS IFORMAITON TECHNLOGIE GE SOLAR 800I PATIENT MONITOR 01/02/2015
PHILIPS MEDICAL SYSTEMS COMPONENT MONITORING SYSTEM 08/26/2014
PHILIPS MEDICAL SYSTEMS V24/26 COMPONENT MONITORING SYSTEM 06/03/2014
PHILIPS MEDICAL SYSTEMS COMPONENT MONITORING SYSTEM (FLATSCREEN) 06/02/2014
PHILIPS MEDICAL SYSTEMS COMPONENT MONITORING SYSTEM 05/05/2014
PHILIPS MEDICAL SYSTEMS V24/26 COMPONENT MONITORING SYSTEM 04/15/2014
-
-