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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience(MAUDE)
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90 records meeting your search criteria returned- Product Code: HQF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ELLEX MEDICAL PTY LTD TANGO 06/07/2024
SIE AG, SURGICAL INSTRUMENT ENGINEERING ZIEMER FEMTO LDV 02/29/2024
ELLEX MEDICAL PTY LTD ULTRA Q REFLEX 12/14/2023
ELLEX MEDICAL PTY LTD ULTRA Q REFLEX 12/14/2023
ELLEX MEDICAL PTY LTD ULTRAQ REFLEX 12/06/2023
ELLEX MEDICAL PTY LTD ULTRA Q REFLEX 11/21/2023
ALCON RESEARCH, LLC - IRVINE TECHNOLOGY PUREPOINT LASER 04/20/2023
IRIDEX CORPORATION G-PROBE 09/30/2022
IRIDEX CORPORATION MICROPULSE P3 DEVICE 08/18/2022
IRIDEX CORPORATION MICROPULSE P3 DEVICE 08/18/2022
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