BEUDAMED
    11 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SYNCARDIA FREEDOM ONBOARD BATTERY

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 19, 2022

    SYNCARDIA FREEDOM ONBOARD BATTERY

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 21, 2022

    STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 24, 2011

    RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

    RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

    RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

    SYRINGE BOIN TUBE 10ML 21G 1-1/4IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·October 13, 2020

    SYNCARDIA FREEDOM BATTERY CHARGER

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 19, 2022

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·February 2, 2016