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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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11 records meeting your search criteria returned- Product Code: IZI Product Problem: Overheating of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. MULTIDIAGNOST ELEVA 11/20/2020
SIEMENS AG/SIEMENS HEALTHCARE GMBH AXIOM ARTIS ZEE 10/26/2018
SIEMENS AG/SIEMENS HEALTHCARE GMBH ARTIS ZEEGO 06/30/2017
PHILIPS HEALTHCARE ALLURA XPER FD10 01/20/2017
SIEMENS HEALTHCARE ARTIS ZEE BIPLANE 01/03/2017
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC AXIOM ARTIS ZEEGO 09/15/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC AXIOM ARTIS ZEE CEILING 07/15/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE FLOOR 07/08/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEEGO 04/13/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC COROSKOP HI-P 02/16/2016
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