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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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16 records meeting your search criteria returned- Product Code: JAA 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 GMBH AXIOM LUMINOS TF 09/28/2023
GE MEDICAL SYSTEMS, LLC PRESTIGE VH 12/10/2020
GE MEDICAL SYSTEMS, LLC PRECISION 500D R&F X-RAY SYSTEM 11/15/2019
MEDTRONIC NAVIGATION, INC (LITTLETON) IMAGING SYSTEM 08/29/2019
GE MEDICAL SYSTEMS, LLC PRECISION 500D R&F X-RAY SYSTEM 05/22/2019
CANON MEDICAL SYSTEMS CORPORATION CANON 03/08/2018
SIEMENS HEALTHCARE GMBH AXIOM LUMINOS AGILE MAX 03/05/2018
SIEMENS HEALTHCARE GMBH AXIOM LUMINOS AGILE 12/21/2017
DORNIER MEDTECH SYSTEMS GMBH DORNIER GENESIS 06/19/2017
TOSHIBA MEDICAL SYSTEMS CORPORATION TOSHIBA 01/20/2017
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