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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
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10 records meeting your search criteria returned- Product Code: IYE Product Problem: Device Handling Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
VARIAN MEDICAL SYSTEMS CALYPSO 09/05/2023
ELEKTA SOLUTIONS AB ELEKTA MEDICAL LINEAR ACCELERATOR 09/01/2023
VARIAN MEDICAL SYSTEMS CLINAC-21EX 08/23/2023
ELEKTA SOLUTIONS AB MOSAIQ 07/01/2022
SIEMENS HEALTHCARE GMBH ARTISTE MV 06/09/2022
ELEKTA INC MOSAIQ 12/03/2021
ACCURAY INCORPORATED RADIXACT 08/26/2019
BRAINLAB AG EXACTRAC 6.2 09/06/2017
BRAINLAB AG EXACTRAC 6.2 06/02/2017
ELEKTA LTD XVI 06/07/2016
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