BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    EYE SPONGE OR SPEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704262230·

    STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TITANIUM M.E. MULLER TYPE TOTAL HIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·July 16, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 28, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 15, 2012

    HUDSON MICRO MIST NEBULIZER W/ELONG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCQ·June 9, 2015

    ECHOTIP ULTRA ULTRASOUND ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·November 19, 2010

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 29, 2014

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·September 17, 2014