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

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    SPECTACLE FRAMES AND SUNGLASSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981058418·17mm Hollywood Trial, Lordotic

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889910058410·17mm Hollywood Trial, Lordotic

    JAKOBI SURG. INSTRUMENTS #6 50

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ECONOMY C-ARM TABLE, MODEL # 056-005

    FDA 510(k)
    FDA Class 2 ·Radiology

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·January 30, 2013

    OCTAD STANDARD LEAD 1X8

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·December 8, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·February 4, 2014