BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    FREESTYLE FREEDOM

    FDA Adverse Event
    Malfunction ·Product code NBW·December 28, 2010

    ALINITY I B12 REAGENT KIT

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code CDD·August 1, 2022

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 26, 2013

    RESTORE PRIME

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 28, 2011

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·March 25, 2008

    SPECTRA OPTIA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code GKT·August 8, 2022

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024

    HEPATIC ARTERY INFUSION PUMP

    FDA Adverse Event
    Injury ·INTERA ONCOLOGY·Product code LKK·March 28, 2023