BEUDAMED
    12 results · 55ms · Sources: EU EUDAMED, US FDA

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    HEARTSINE GATEWAY 500P BUNDLE SALES BOM - UK ENGLISH

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·January 28, 2025

    HEARTSINE SAMARITAN 350P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·May 31, 2017

    HEARTSINE SAMARITAN 300P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·June 19, 2018

    HEARTSINE SAMARITAN 300P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·August 30, 2019

    3004123209-2018-00506

    FDA Adverse Event
    Death ·August 6, 2018

    HDF3500 AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·August 10, 2020

    BATTERY,PAD-PAK-01

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·May 21, 2019

    OB CO#1310451,PKG,350P,PP01,EN,350-BAS-US-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·March 12, 2020

    HEARTSINE TECHNOLOGIES SAMARITAN 300/300P PAD PUBLIC ACCESS DEFIBRILLATORS

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES INC·Product code MKJ·September 19, 2013

    HeartSine Samaritan AED Defibrillators Models: SAM 001, SAM 002, SAM 003.

    FDA Recall
    Terminated ·Heartsine Technologies Inc·Product code MKJ·October 5, 2005

    Heartsine Samaritan AED Defibrillators - Models: SAM 001, SAM 002, SAM 003. Serial numbers within range of 1270 - 2324 (not all are affected).

    FDA Recall
    Terminated ·Heartsine Technologies Inc·Product code MKJ·February 14, 2005

    SAMARITAN AED PADS

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD. BELFAST, N.I. BY KATECHO INC.·Product code MLN·January 8, 2005