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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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133 records meeting your search criteria returned- Product Code: IYE Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SIEMENS HEALTHINEERS GMBH ARTISTE MV SYSTEM 07/21/2017
SIEMENS HEALTHCARE GMBH AT-RO ONCOR IMPRESSION PLUS 05/23/2017
SIEMENS HEALTHCARE GMBH AT-RO PRIMUS HI 05/18/2017
SIEMENS HEALTHCARE GMBH AT-RO ARTISTE MV SYSTEM 04/13/2017
SIEMENS HEALTHCARE GMBH AT-RO RT THERAPIST 4.3.1_MR2 04/11/2017
MEDICAL INTELLIGENCE FRAXION 02/21/2017
ACCURAY INCORPORATED ACCURAY TOMOTHERAPY HI-ART SYSTEM 01/13/2017
SIEMENS HEALTHCARE GMBH ONCOR IMPRESSION PLUS 01/04/2017
IMPAC MEDICAL SYSTEMS, INC. MOSAIQ 12/14/2016
IMPAC MEDICAL SYSTEMS, INC. MOSAIQ 12/02/2016
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