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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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90 records meeting your search criteria returned- Product Code: IZI Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
PHILIPS HEALTHCARE ALLURA XPER FD10 04/09/2018
GE MEDICAL SYSTEMS INNOVA 01/02/2018
PHILIPS MEDICAL SYSTEMS PHILLIPS C-ARM ALLURA XPER FD 10 07/20/2017
TOSHIBA MEDICAL SYSTEMS CORPORATION INFINIX 07/11/2017
PHILIPS HEALTHCARE ALLURA XPER FD10 06/28/2017
SIEMENS AG/SIEMENS HEALTHCARE GMBH ARTIS BIPLANE C-ARM SYSTEM 05/05/2017
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE BIPLANE 03/21/2017
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE MULTI-PURPOSE 03/17/2017
PHILIPS HEALTHCARE INTEGRIS ALLURA 9 03/14/2017
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE BIPLANE 03/07/2017
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