• 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 
 
 
11 records meeting your search criteria returned- Product Code: DRG Product Problem: Device Stops Intermittently Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NKUS LAB CENTRAL MONITORING SYSTEM 10/09/2016
NIHON KOHDEN CORPORATION CENTRAL MONITORING SYSTEM 02/25/2016
NIHON KOHDEN CORPORATION ORG-9700A 11/16/2015
NIHON KOHDEN CORPORATION ORG-9110A 12/24/2014
NIHON KOHDEN CORPORATION ORG-9100A 12/24/2014
Unknown Manufacturer ORG-9110A 12/24/2014
NIHON KOHDEN CORPORATION ORG-9100A 12/24/2014
NIHON KOHDEN CORPORATION ZM-920PA 12/17/2014
NIHON KOHDEN CORPORATION ZM-920PA 12/17/2014
NIHON KOHDEN CORPORATION ORG-9100A 08/12/2014
-
-