BEUDAMED
    38 results · 25ms · Sources: EU EUDAMED, US FDA

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    6000023-2013-00008

    FDA Adverse Event
    Injury ·VITATRON MEDICAL B.V.·Product code NVY·February 15, 2013

    6000023-1997-00061

    FDA Adverse Event
    Injury ·September 10, 1997

    6000023-1998-00039

    FDA Adverse Event
    Product code LWS·July 10, 1998

    6000023-1999-00068

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00075

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00076

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00072

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00078

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00073

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00081

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00069

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00080

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00074

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00077

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00071

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00070

    FDA Adverse Event
    Malfunction ·November 12, 1999

    6000023-1999-00079

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00064

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00061

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00058

    FDA Adverse Event
    Injury ·September 8, 1999