BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    ACCULITE(TM) OTOPROBE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Nu-Edge Cobalt Chromium Brackets

    FDA UDI
    TP ORTHODONTICS INC·00192029045848·UL BI W/HK

    ECLIPSE

    FDA 510(k)
    FDA Class 2 ·Radiology

    FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM; S.M.A.R.T. RE-FLEX BILIARY ELF-EXPANDING STENT SYSTEM

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

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 28, 2013

    UNKNOWN DEPUY SROM LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·December 14, 2010

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 13, 2014