BEUDAMED
    4 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 23, 2010

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 15, 2013

    MEGA NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 29, 2014

    HYGENIC

    FDA Adverse Event
    Injury ·COLTENE WHALEDENT INC.·Product code EEF·June 2, 2022