BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    Persona Partial Knee

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HI-TORQUE PROCEED Guide Wire Family

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BEMER Classic Set, BEMER Pro-Set

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SPECTRANETICS LEAD LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·SPECTRANETICS CORPORTATION·Product code DRB·November 14, 2014

    SETROX S 45

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO, KG·Product code NVZ·August 10, 2011

    CORMET RESURFACING

    FDA Adverse Event
    CORIN LTD.·Product code NXT·July 24, 2013