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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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34 records meeting your search criteria returned- Product Code: IZI Product Problem: Device Inoperable Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS INC. PHILIPS X-RAY 05/02/2018
SIEMENS MEDICAL SOLUTIONS USA, INC. AXIOM ARTIS 01/10/2018
PHILIPS HEALTHCARE ALLURA XPER FD10 11/16/2017
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEEGO 09/01/2016
PHILIPS MEDICAL SYSTEMS ALLURA XPER FD20/10 08/31/2016
PHILIPS HEALTHCARE ALLURA XPER FD10 07/20/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEEGO 07/08/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE BIPLANE 06/01/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEEGO 04/13/2016
PHILIPS HEALTHCARE ALLURA XPER FD10 04/12/2016
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