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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 3, 2012

    ALARIS PUMP MODULE SET NON-VENTED BLOOD SET

    FDA Adverse Event
    Malfunction ·Product code FPA·June 29, 2021

    BD ALARIS¿ LVP BLD180M 15D SS

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 30, 2020