BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 7, 2022

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 7, 2022

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·November 19, 2015

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 10, 2018

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·April 28, 2014

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 20, 2013

    OMNISPAN MENISCAL FASTENER, 12 DEGREE NEEDLE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MBI·January 14, 2011

    LVIS JR.

    FDA Adverse Event
    Injury ·MICROVENTION INC.·Product code QCA·June 18, 2024

    LVIS EVO

    FDA Adverse Event
    Death ·MICROVENTION, INC.·Product code NJE·August 19, 2022

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·September 7, 2022