• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
239 records meeting your search criteria returned- Product Code: NAW Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOCOMPATIBLES UK LTD THERASPHERE 05/04/2020
BIOCOMPATIBLES UK LTD THERASPHERE 04/14/2020
BIOCOMPATIBLES UK LTD THERASPHERE 04/07/2020
BIOCOMPATIBLES UK LTD THERASPHERE 03/25/2020
BIOCOMPATIBLES UK LTD THERASPHERE 03/24/2020
BIOCOMPATIBLES UK LTD THERASPHERE 03/10/2020
BIOCOMPATIBLES UK LTD THERASPHERE 03/09/2020
BIOCOMPATIBLES UK LTD THERASPHERE 03/03/2020
SIRTEX TECHNOLOGY PTY LTD SIR-SPHERES® Y-90 RESIN MICROSPHERES 02/21/2020
SIRTEX TECHNOLOGY PTY LTD SIR-SPHERES® Y-90 RESIN MICROSPHERES 02/21/2020
-
-