BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    RANGE OF NEUROSURGICAL INSTRUMENTS IN TITANIUM

    FDA 510(k)
    FDA Class 1 ·Neurology

    MINIDEF (OR DEFIPORT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sorrento Bioglass Bone Graft Substitute

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 5, 2014

    TELIGEN

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

    120 RELIANCE CART WASHER

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code LDS·December 14, 2012