BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RUMI II KOH-EFFICIENT

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·October 20, 2022

    BD ANGIOCATH¿ IV CATHETER 22 G X 1"

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017

    KOH-EFFICIENT,RUMI

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·November 4, 2022

    KOH-EFFICIENT,RUMI

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·November 3, 2022

    EON MINI

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL NEUROMODULATION·Product code GZB·June 19, 2014

    CRW BIOPSY PLUS

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·February 6, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CLONMEL IRELAND·Product code NVZ·January 6, 2011

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017