BEUDAMED
    6 results · 17ms · 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.

    MCGHAN LONGTERM MAMMARY EXPANDER, RTV DESIGN

    FDA 510(k)
    FDA Unclassified ·Unknown

    JAKOBI SURG. INSTRUMENTS #11 14/45

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

    MODIFIED C-DAK

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code MCX·June 10, 2014

    VITALITY

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 11, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012