BEUDAMED
    9 results · 17ms · 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 ×

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 9, 2025

    PRE-SHAPED PROWLER MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·March 20, 2013

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·March 12, 2008

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 19, 2026

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 19, 2026

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 19, 2026

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 19, 2026

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 19, 2026

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 19, 2026