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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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17 records meeting your search criteria returned- Product Code: DHX Product Problem: No Apparent Adverse Event Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 05/18/2020
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 05/18/2020
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 05/18/2020
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 05/18/2020
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 12/23/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ATTELLICA IM CARCINOEMBRYONIC ANTIGEN (C 10/10/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 06/28/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XPT CEA 05/30/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 03/14/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CEA ASSAY 11/16/2018
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