BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ODYSSEY

    FDA Adverse Event
    Malfunction ·PERMEDICS, INC.·Product code MUJ·November 4, 2010

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·January 9, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 7, 2014

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023

    RADIFOCUS ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018