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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
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11 records meeting your search criteria returned- Product Code: MOI Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE/IMMULITE 1000 BR-MA 11/17/2017
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE 2000/IMMULITE 2000 XPI BR-MA 11/17/2017
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE 2000 BR-MA 04/04/2017
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP BR (27.29 ) ASSAY 01/23/2017
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE 2000 BR-MA 10/14/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR XP 06/08/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR 06/07/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XPT CA 15-3 ASSAY 03/18/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA CENTAUR BR (27.29) 02/17/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. IMMULITE 2000 BR-MA 01/08/2016
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