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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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15 records meeting your search criteria returned- Product Code: JAA Patient Problem: Fall Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
GE MEDICAL SYSTEMS, LLC PRECISION 500D R&F X-RAY SYSTEM 05/22/2019
GE MEDICAL SYSTEMS, LLC PRECISION 500D 06/25/2018
SIEMENS SIEMENS SIRESKOP SD 03/15/2018
CANON MEDICAL SYSTEMS CORPORATION CANON 03/06/2018
GE MEDICAL SYSTEMS, LLC PRECISION 500D 02/05/2018
TOSHIBA MEDICAL SYSTEMS CORPORATION TOSHIBA 01/20/2017
SIEMENS GMBH LUMINOS AGILE MAX 04/08/2016
SIEMENS HEALTHCARE GMBH AXIOM LUMINOS AGIE 06/10/2015
GE MEDICAL SYSTEMS, LLC PRESTIGE VH 04/16/2015
SIEMENS AG AXIOM LUMINOS TF 03/30/2015
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