BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 6, 2011

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 22, 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