BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    PULSOR, THERAPEUTIC VIBRATOR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Legacy™4 Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307103004·Ø4.7 x 16 Platform 4.5mmD

    MAGNIFYING SPECTACLES W/PLASTIC LENSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NSI ASTRA TM CALCIUM REAGENT KIT NSI ITEM # 7909

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 24, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 19, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·December 15, 2012