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

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    Filters FDA Adverse Event ×

    CONNECTOR LUER LOCK C45J

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code LHI·September 11, 2019

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·April 10, 2014

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·October 31, 2012

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·August 17, 2010