BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    BAG SPIGOT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756371162·ORTHO PACK

    HI VISION ASCENDUS DIAGNOSTIC ULTRASOUND SCANNER

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARTHREX FIBERWIRE, MODEL SPU-02NB-3800

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

    EXPEDIUM 6.35 TITANIUM SET SCREW

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code MNH·November 22, 2010

    CONTAK RENEWAL TR

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NKE·January 11, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·July 2, 2014