BEUDAMED
    4 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·July 23, 2020

    ECHELON FLEX 60

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY·Product code GDW·January 8, 2013

    QUICKIE 2 LITE

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL (US) LLC·Product code IOR·November 17, 2010

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·July 2, 2014