BEUDAMED
    3 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A-38 CUP NON FLARED SZ 60MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 8, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014

    PENTA SURGICAL LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL -NEUROMODULATION·Product code LGW·January 13, 2011