BEUDAMED
    3 results · 45ms · 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 ×

    PRISMAFLEX

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·August 24, 2022

    PRISMA

    FDA Adverse Event
    Malfunction ·GAMBRO [RENAL PRODUCTS]·Product code FJK·May 23, 2003

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·February 5, 2020