BEUDAMED
    6 results · 119ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NEUVIZ DUAL

    FDA Adverse Event
    Malfunction ·PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Product code JAK·February 12, 2010

    MX 16-SLICE

    FDA Adverse Event
    PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Product code JAK·March 15, 2013

    NEUVIZ 16

    FDA Adverse Event
    Malfunction ·PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Product code JAK·February 11, 2011

    NEUVIZ DUAL

    FDA Adverse Event
    Malfunction ·PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Product code JAK·November 30, 2007

    MX 16-SLICE

    FDA Adverse Event
    PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Product code JAK·October 19, 2012

    NEUVIZ DUAL

    FDA Adverse Event
    Malfunction ·PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Product code JAK·May 30, 2008