BEUDAMED
    5 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 1, 2013

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·February 28, 2011

    GE OEC 9900

    FDA Adverse Event
    Injury ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·April 23, 2008

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·May 7, 2025

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·.·Product code KWA·May 19, 2017