BEUDAMED
    3 results · 15ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 5, 2011

    23GA ILLUMINATED DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·March 19, 2020

    25GA ILLUMINATED DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·March 19, 2020