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

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    KSEA BIPOLAR GOAGULATING FORCEPS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DRILL SLEEVE F. SOLID STEPDRILL

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·February 23, 2012

    SILK Surgical Suture

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

    MODIFICATION TO STOCKERT S5 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 14, 2013

    ASR ACETABULAR CUPS 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014