• 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
 

 
 
 1 
 2 
 3 
 > 
 
24 records meeting your search criteria returned- Product Code: MOI Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS ELECSYS CA 15-3 II 02/08/2021
ROCHE DIAGNOSTICS ELECSYS CA 15-3 II ASSAY 03/14/2017
ROCHE DIAGNOSTICS COBAS 6000 E 601 MODULE 02/10/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 04/03/2015
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 03/20/2015
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR 03/19/2015
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP 02/13/2015
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR 02/13/2015
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR 01/29/2015
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 01/09/2015
-
-