BEUDAMED
    6 results · 63ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEARTSINE SAMARITAN 300P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·May 15, 2018

    PACKAGE,350P,PP01,EN,350-BAS-US-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·December 3, 2019

    HEARTSINE SAMARITAN 350P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·January 8, 2018

    PACKAGE,350P,PP01,EN,350-STR-US-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·September 10, 2024

    PACKAGE,350P,PP03,INTL EN,350-BAS-UK-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code NSA·October 30, 2024

    PACKAGE,500P,PP03,INTL EN,500-BAS-UK-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·June 26, 2020