BEUDAMED
    27 results · 65ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code NOU·October 1, 2014

    E200

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·May 22, 2000

    NEWPORT HT50 VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 5, 2005

    E500 VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·January 6, 2014

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·January 8, 2014

    E500 VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·September 2, 2011

    HT70 VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 15, 2013

    E200

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·July 25, 1997

    E200

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·September 26, 1997

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code NOU·September 8, 2014

    E100I NEWPORT VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·November 7, 2005

    NEWPORT HT50

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 2, 2003

    E100I

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·December 15, 1999

    E360 VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·March 16, 2016

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·January 26, 2017

    HT70

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·July 22, 2013

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·August 30, 2013

    E150

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·October 19, 1998

    E200

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·December 31, 1998

    HT50 VENTILATOR

    FDA Adverse Event
    Death ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·January 29, 2018