BEUDAMED
    5 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEPTH DEVICE, 2.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 16, 2023

    DEPTH DEVICE, 2.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·April 23, 2024

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 6, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·October 13, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 19, 2012