• 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 
 4 
 5 
 6 
 > 
 
60 records meeting your search criteria returned- Product Code: MHX Product Problem: Image Display Error/Artifact Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION CNS-6201A 06/13/2017
PHILIPS MEDICAL SYSTEMS VM6 05/31/2017
PHILIPS MEDICAL SYSTEMS INTELLIVUE 03/28/2017
SPACELABS HEALTHCARE INC. SPACELABS XHIBIT CENTRAL STATION 12/23/2016
PHILIPS MEDICAL SYSTEMS INTELLIVUE MX800 PATIENT MONITOR 12/07/2016
PHILIPS MEDICAL SYSTEMS PHILIPS EFFICIA CMS200 CENTRAL MONITORIN 11/11/2016
NIHON KOHDEN TOMIOKA CORPORATION BSM-6300A 05/13/2016
NIHON KOHDEN CORPORATION BSM-2351A 03/30/2016
NIHON KOHDEN TOMIOKA CORPORATION BSM-2354A 01/10/2016
NIHON KOHDEN CORPORATION RNS-9703-019 01/02/2016
-
-