BEUDAMED
    9 results · 58ms · 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 FDA Adverse Event ×

    NICOLET VEEG SYSTEM

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORATED·Product code GWQ·September 10, 2015

    LUMBAR DRAINAGE CATH II KIT LAWSON

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY INC.·Product code CAZ·February 7, 2019

    NATUS DISPOSABLE DISC ELECTRODES

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORTAED·Product code GXY·July 21, 2015

    NICOLET CORTICAL STIMULATOR

    FDA Adverse Event
    Malfunction ·NATUS NEUROLOGY, INCORPORATED·Product code GYC·September 10, 2015

    NATUS DISPOSABLE DISC ELECTRODES

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORTAED·Product code GXY·July 30, 2015

    NATUS DISPOSABLE DISC ELECTRODES

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORATED·Product code GXY·August 11, 2015

    NATUS DISPOSABLE DISC ELECTRODES

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORTAED·Product code GXY·August 12, 2015

    NATUS DISPOSABLE DISC ELECTRODES

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORTAED·Product code GXY·August 12, 2015

    NATUS DISPOSABLE DISC ELECTRODES

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORTAED·Product code GXY·August 12, 2015