BEUDAMED
    5 results · 20ms · 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 ×

    LIBERTY POSTERIOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·July 29, 2014

    EQUINOXE CAGE GLENOID M, POST AUG, LEFT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·October 2, 2024

    GYNECARE PROLIFT PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON SARL·Product code OTP·July 29, 2015

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 22, 2014

    ALTERNATE BEARING METAL LINER 28MM I.D.

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 6, 2011