• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECKMAN COULTER COULTER ACT 10/04/2019
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 360/560 DILUENT 10/04/2019
ABBOTT DIAGNOSTICS DIVISION CELL-DYN SAPPHIRE ANALYZER 10/01/2019
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 2120 HEMATOLOGY SYSTEM WITH SINGLE 09/12/2019
ABBOTT DIAGNOSTICS DIVISION CELL-DYN SAPPHIRE ANALYZER 09/04/2019
BECKMAN COULTER UNICEL DXH 800 COULTER CELLULAR ANALYSIS 09/04/2019
ABBOTT DIAGNOSTICS DIVISION CELL-DYN SAPPHIRE ANALYZER 09/03/2019
ABBOTT DIAGNOSTICS DIVISION CELL-DYN RUBY ANALYZER 09/02/2019
ABBOTT DIAGNOSTICS DIVISION CELL-DYN RUBY ANALYZER 08/23/2019
ABBOTT DIAGNOSTICS DIVISION CELL-DYN EMERALD ANALYZER 08/15/2019
-
-