BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    13X75 MM 4.0 ML BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·July 27, 2017

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 3, 2018

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 3, 2018

    VITALITY 2 VR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    SECURE 3 MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·August 10, 2011

    MBT CEM KEEL TIB TRAY SZ5

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code NJL·July 30, 2013

    13X75 MM 4.0 ML BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO.·Product code JKA·July 25, 2017

    13X75 MM 4.0 ML BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO.·Product code JKA·July 25, 2017