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

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ManufacturerBrand NameDate Report Received
CANON MEDICAL SYSTEMS CORPORATION CANON 05/25/2021
ANGIODYNAMICS, INC. NAMIC SQUEEZE CONTRAST CONTROLLER 09/09/2019
PHILIPS HEALTHCARE INTEGRIS CV (CESAR-POWERPACK-VISUB-NICOL 10/23/2018
SIEMENS HEALTHCARE GMBH- AT ARTIS ZEEGO Q 02/15/2018
SIEMENS HEALTHCARE GMBH- AT ARTIS ZEEGO Q 02/15/2018
PHILIPS HEALTHCARE ALLURA XPER FD10 11/28/2017
SIEMENS MEDICAL SOLUTIONS USA, INC. ARTIS ZEE CEILING 01/06/2015
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