Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
19 records meeting your search criteria returned- Product Code: LOL 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
ABBOTT GERMANY ARCHITECT HAVAB-G 07/23/2018
ABBOTT GERMANY ARCHITECT HAVAB-G 07/23/2018
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR CP HAV TOTAL (AHAVT) ASSAY 02/16/2017
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP HAV TOTAL (AHAVT) ASSAY 02/09/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 01/30/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR CP 12/09/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP HAV TOTAL (AHAVT) ASSAY 11/22/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR CP HAV TOTAL (AHAVT) ASSAY 11/03/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 11/03/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR CP HAV TOTAL (AHAVT) 08/12/2016
-
-