BEUDAMED
    12 results · 113ms · Sources: EU EUDAMED, US FDA

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    GEMINI GXL 16 POWER

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code KPS·March 16, 2010

    GYROSCAN ACS-NT

    FDA Adverse Event
    Other ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code LNH·July 20, 2000

    NI

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code ITY·April 7, 2000

    PHILIPS

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code JAA·May 27, 1999

    PICKER CLINIX PLUS

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code JAA·May 20, 2011

    PHILIPS HEARTSTART MRX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code MKJ·February 4, 2020

    PHILIPS HEARTSTART XL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code MKJ·March 27, 2020

    PHILIPS INTELLIVUE MP50 PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code MHX·January 24, 2020

    PHILIPS HEARTSTART XL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code MKJ·March 18, 2020

    PHILIPS M3002A X2 MONITOR/MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code MHX·August 19, 2019

    PHILIPS INTELLIVUE MP5 PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.·Product code MHX·August 19, 2019

    PHILIPS 1.5T INTERA

    FDA Adverse Event
    Injury ·PHILIPS MEDICAL SYSTEMS NORTH AMERICA INC.·Product code LNH·September 23, 2010