BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 28, 2026

    EDGE

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO HEALTHCARE·Product code GEI·July 22, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 20, 2013

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·October 15, 2014

    SKINTACT

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code DRX·January 21, 2019

    SKINTACT

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code MKJ·June 19, 2019

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 9, 2019