BEUDAMED
    12 results · 52ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SIEMENS SENSIS

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code MHX·July 21, 2005

    NONIN WRISTOX2 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL INC.·Product code DQA·June 27, 2016

    9843

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code CCK·January 17, 2002

    MODEL 8000CA

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code MUD·October 27, 2009

    MODEL 7600B

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code DQA·October 28, 2009

    PURELIGHT SENSORS

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC·Product code DQA·October 6, 2010

    PURELIGHT

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC·Product code DQA·October 19, 2010

    RESPSENSE

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code CCK·June 18, 2019

    RESPSENSE

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code CCK·October 2, 2011

    NONIN 8500

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL INC·Product code DQA·November 15, 2004

    NONIN

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code DQA·March 31, 2022

    WRISTOX2 PULSE OXIMETER BLE

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC.·Product code DQA·February 17, 2022