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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
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3 records meeting your search criteria returned- Product Code: IYE Product Problem: Human Factors Issue Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SIEMENS HEALTHINEERS GMBH PRIMUS HI 05/18/2018
BRAINLAB AG EXACTRAC 6.2 06/02/2017
VARIAN MEDICAL SYSTEMS VARIAN CLINAC IX 02/29/2016
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