BEUDAMED
    6 results · 46ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GXDP-700

    FDA Adverse Event
    Malfunction ·PALODEX GROUP OY·Product code MUH·June 5, 2012

    DIGORA OPTIME

    FDA Adverse Event
    Malfunction ·PALODEX GROUP OY·Product code EHD·December 16, 2021

    GENDEX

    FDA Adverse Event
    Malfunction ·PALODEX GROUP OY·Product code EHD·July 13, 2022

    FOCUS

    FDA Adverse Event
    Malfunction ·PALODEX GROUP OY·Product code EHD·December 2, 2022

    GXDP-300

    FDA Adverse Event
    Injury ·PALODEX GROUP OY·Product code MUH·June 2, 2017

    GXDP-300

    FDA Adverse Event
    Injury ·PALODEX GROUP OY·Product code MUH·June 2, 2017