BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 11, 2013

    WECK HEM-O-LOK CLIPS, LARGE

    FDA Adverse Event
    Injury ·TELEFLEX MEDICAL·Product code FZP·January 10, 2011

    UNIPLANAR SCREW (TI-6AL-4V)

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code KWP·July 28, 2014