• 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
 

 
 
9 records meeting your search criteria returned- Product Code: MOI Report Date From: 1/1/2016 Report Date To: 12/31/2016

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE 2000 BR-MA 10/14/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR CP 07/19/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 06/08/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR 06/07/2016
ROCHE DIAGNOSTICS ELECSYS CA 15-3 03/21/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XPT CA 15-3 ASSAY 03/18/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 03/03/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR BR (27.29) 02/17/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. IMMULITE 2000 BR-MA 01/08/2016
-
-