BEUDAMED
    3 results · 13ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    NONE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code UNK·December 11, 2009

    TENOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·December 11, 2009

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWP·August 8, 2014