BEUDAMED
    12 results · 46ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ARTOSCAN

    FDA Adverse Event
    Death ·ESAOTE S.P.A.·Product code LNH·May 25, 2001

    ARTOSCAN

    FDA Adverse Event
    Death ·ESAOTE S.P.A.·Product code LNH·December 22, 2000

    ECG SYSTEMS

    FDA Adverse Event
    Malfunction ·ESAOTE S.P.A.·Product code DRT·December 30, 2003

    C-SCAN

    FDA Adverse Event
    Other ·ESAOTE S.P.A.·Product code LNH·December 23, 2003

    MYL

    FDA Adverse Event
    Malfunction ·ESAOTE S.P.A.·Product code IYN·May 4, 2005

    ECG SYSTEMS

    FDA Adverse Event
    Malfunction ·ESAOTE S.P.A.·Product code DRT·May 3, 2004

    ECG SYSTEMS

    FDA Adverse Event
    Malfunction ·ESAOTE S.P.A.·Product code DRT·May 3, 2004

    ECG SYSTEMS

    FDA Adverse Event
    Malfunction ·ESAOTE, S.P.A.·Product code DRT·May 3, 2004

    ECG SYSTEMS

    FDA Adverse Event
    Malfunction ·ESAOTE, S.P.A.·Product code DRT·May 3, 2004

    ECG SYSTEMS

    FDA Adverse Event
    Malfunction ·ESAOTE, S.P.A.·Product code DRT·May 3, 2004

    ESCAN XQ

    FDA Adverse Event
    Injury ·ESAOTE S.P.A.·Product code LNH·May 23, 2008

    ESAOTE

    FDA Adverse Event
    Malfunction ·ESAOTE S.P.A.·Product code IYN·December 20, 2013