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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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13 records meeting your search criteria returned- Product Code: HNQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 01/16/2020
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 04/18/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 03/26/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 03/26/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 02/07/2019
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 11/15/2018
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 09/05/2018
IANTECH, INC. LOW ENERGY ENDOCAPSULAR PHACO (LEEP) DEV 06/05/2018
IANTECH, INC. LOW ENERGY ENDOCAPSULAR PHACO (LEEP) DEV 01/23/2018
IANTECH, INC. LOW ENERGY ENDOCAPSULAR PHACO (LEEP) DEV 12/19/2017
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