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

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    Filters FDA Adverse Event ×

    PLEXUR M

    FDA Adverse Event
    Injury ·OSTEOTECH, INC. (SUBSIDIARY OF MEDTRONIC)·Product code MQV·December 3, 2013

    PLEXUR M

    FDA Adverse Event
    Injury ·OSTEOTECH, INC.·Product code MQV·December 29, 2010

    MAXFRAME AUTOSTRUT(TM)HEXAPOD STRUT-MED

    FDA Adverse Event
    Malfunction ·SYNTHES TRAUMA : ORTHOSPIN·Product code KTT·January 23, 2025

    LASE MODEL 1100-010

    FDA Adverse Event
    Other ·CLARUS MEDICAL, LLC.·Product code GEX·December 26, 2001

    PLEXUR M

    FDA Adverse Event
    Injury ·OSTEOTECH, INC (SUBSIDIARY OF MEDTRONIC)·Product code MQV·June 20, 2013

    2.1MM CROSS-CUT FISSURE EXTENDED

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBE·December 11, 2018

    PLEXUR M

    FDA Adverse Event
    Injury ·OSTEOTECH, INC (SUBSIDIARY OF MEDTRONIC)·Product code MQV·December 9, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 8, 2013

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 18, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·May 23, 2011

    TPS ELITE LONG ATTACHMENT

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS·Product code HBF·January 19, 2007