• 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 
 > 
 
44 records meeting your search criteria returned- Product Code: DRG Report Date From: 1/1/2022 Report Date To: 12/31/2022

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC. WI-BOX¿ WIRELESS SOLUTION 12/22/2022
ST. JUDE MEDICAL, INC WI-BOX 12/22/2022
COVIDIEN MFG DC BOULDER VITAL SYNC REMOTE MONITORING SYSTEM 12/21/2022
COVIDIEN MFG DC BOULDER VITAL SYNC REMOTE MONITORING SYSTEM 11/29/2022
NIHON KOHDEN CORPORATION ORG-9110A 10/25/2022
NIHON KOHDEN CORPORATION ORG-9110A 10/12/2022
NIHON KOHDEN CORPORATION NI 08/27/2022
COVIDIEN MFG DC BOULDER VITAL SYNC REMOTE MONITORING SYSTEM 08/18/2022
NIHON KOHDEN CORPORATION ORG-9110A 08/05/2022
NIHON KOHDEN CORPORATION ORG-9110A 07/21/2022
-
-