BEUDAMED
    54 results · 72ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    MEE-1000A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code GWF·March 21, 2016

    ZM-530PA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code DRT·November 9, 2016

    SIEMENS MEDICAL

    FDA Adverse Event
    Injury ·NIHON KOHDEN AMERICA INC·Product code MHX·January 20, 2009

    CNS-6201

    FDA Adverse Event
    NIHON KOHDEN AMERICA, INC.·Product code MHX·June 18, 2014

    CNS-6201

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·October 6, 2014

    CNS-9700

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·August 12, 2015

    TELEVISION MONITOR

    FDA Adverse Event
    Death ·NIHON KOHDEN AMERICA, INC.·Product code MHX·December 9, 2009

    *

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA INC·Product code GWF·May 16, 2005

    PULSE OXIMETRY PROBE

    FDA Adverse Event
    NIHON KOHDEN AMERICA, INC.·Product code DQA·March 12, 2014

    NIHON KOHDEN LIFE SCOPE G7

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·October 16, 2025

    RADIANCE SATELLITE

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·May 30, 2013

    CARDIOLIFE

    FDA Adverse Event
    Injury ·NIHON KOHDEN (AMERICA), INC.·Product code LDD·November 23, 1994

    NOHON KOHDEN, EEG

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code GWS·December 23, 1996

    NIHON KOHDEN PATIENT MONITOR

    FDA Adverse Event
    Injury ·NIHON KOHDEN AMERICA, INC.·Product code MHX·October 25, 2018

    NIHON KOHDEN

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·August 21, 2025

    NIHON KOHDEN

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·August 21, 2025

    NIHON KOHDEN

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·August 21, 2025

    NIHON KOHDEN

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code DRG·August 21, 2025

    *

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code DRG·February 17, 2011

    NIHON KOHDEN

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN AMERICA, INC.·Product code MHX·March 10, 2023