BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    AEROQUIP SAFESTART IV CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970669·anteriors; shade D2 light; mould CS

    IOL INJECTOR SET

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Insulia Diabetes Management Companion

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ROOT CANAL INSTRUMENT

    FDA Adverse Event
    Other ·MICRO-MEGA SA·Product code EKS·January 25, 2010

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 5, 2015

    GORE EXCLUDER THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·January 19, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 31, 2014