BEUDAMED
    6 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BD NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 23, 2024

    ZELTIQ COOLMAX (8.0)

    FDA Adverse Event
    Injury ·ZELTIQ AESTHETICS, INC.·Product code OOK·April 18, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 28, 2011

    SENSIA SR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NVZ·July 10, 2008

    ELECSYS FREE PSA

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MTG·November 18, 2024

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 9, 2023