BEUDAMED
    12 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·December 8, 2014

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·December 8, 2014

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·December 8, 2014

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·October 14, 2014

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 16, 2023

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·October 14, 2014

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 6, 2014

    INTEGRATED APD SET W/CASSETTE3 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 22, 2010

    TURBOHAWK ® PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Injury ·EV3 INC.·Product code MCW·December 19, 2012

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·April 26, 2022

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·October 14, 2014

    THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·November 27, 2024