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

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    Filters FDA Adverse Event ×

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·April 10, 2013

    ANGIO-SEAL DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·April 6, 2011

    APEX MODULAR HIP STEM

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE INC.·Product code KWY·May 22, 2008

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·December 10, 2010

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019