BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·February 27, 2013

    HEARTMATE II LVAD

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 15, 2011

    D-TRON PLUS

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·March 31, 2008

    STERILE FX25REC W/RES

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·August 28, 2023

    RANGER PACLITAXEL-COATED PTA BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ONU·August 3, 2023

    MEDTRONIC NAVIGATION

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC·Product code GEX·May 30, 2023