BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NEOCIF INSERTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·November 6, 2018

    NEOCIF INSERTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·July 20, 2017

    PREPMATE ACCESSORY

    FDA Adverse Event
    Malfunction ·TRIPATH IMAGING, INC.·Product code MKQ·September 25, 2008

    PREPMATE ACCESSORY

    FDA Adverse Event
    Malfunction ·TRIPATH IMAGING, INC.·Product code MKQ·August 6, 2008

    PREPMATE ACCESSORY

    FDA Adverse Event
    Malfunction ·TRIPATH IMAGING, INC·Product code MKQ·July 8, 2009

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 29, 2013

    OLYMPUS/GYRUS ACMI

    FDA Adverse Event
    Malfunction ·GYRUS ACMI·Product code FAS·March 10, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·April 21, 2008

    EVOLUT FX VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·August 27, 2025