BEUDAMED
    13 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: Injury ×

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·March 17, 2011

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 1, 2008

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·September 29, 2022