• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
150 records meeting your search criteria returned- Product Code: DXC Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO MEDICAL CORPORATION UNK TR BAND 07/17/2019
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., L VASC BAND 06/27/2019
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., L VASC BAND 06/27/2019
MERIT MEDICAL SYSTEMS INC. PRELUDESYNC¿.RADIAL COMPRESSION DEVICE 06/21/2019
TERUMO MEDICAL CORPORATION TR BAND 05/03/2019
TERUMO MEDICAL CORPORATION UNK TR BAND 04/26/2019
MERIT MEDICAL SYSTEMS INC. PRELUDESYNC¿.RADIAL COMPRESSION DEVICE 04/19/2019
MERIT MEDICAL SYSTEMS INC. PRELUDE SYNC RADIAL COMPRESSION DEVICE 02/08/2019
TERUMO MEDICAL CORPORATION TR BAND 11/15/2018
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., L VASC BAND 10/24/2018
-
-