BEUDAMED
    5 results · 32ms · 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 ×

    7.0MM TI MATRIX REDUCTION SCREW 50MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·August 24, 2015

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    EVA BAG-500ML

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SAO PAULO·Product code BTC·October 7, 2010

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code MUZ·December 6, 2012

    7.0MM TI MATRIX REDUCTION SCREW 50MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·September 8, 2015