BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    CENTRAL LINE TRAY

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EXACTECH ZIRAMIC FEMORAL HEAD COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASSESS(TM) LOW ABNORMAL CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    TOTAL ASR ACET IMP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·January 30, 2013

    OVAL BURR, 12 FLUTE, 5.5MM X 13CM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GFF·December 13, 2010

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·July 15, 2014

    EVOLUT FX VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·November 5, 2025