BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    KEISEI SCALPEL (STERILE AND NON-STERILE)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Legacy™3 Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307102410·3.2mmD x 13mmL, 3.0mmD Platform

    EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDER FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Revolution CT

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·June 10, 2014

    MAXIMO VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code LWS·October 9, 2010

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 10, 2012