BEUDAMED
    378 results · 53ms · Sources: EU EUDAMED, US FDA

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    TOSHIBA MEDICAL SYSTEMS

    FDA Adverse Event
    Injury ·Product code JAK·March 31, 1998

    CT BRAIN PERFUSION (4D BRAIN PERFUSION)

    FDA Adverse Event
    Malfunction ·VITAL IMAGES, INC·Product code LLZ·January 31, 2018

    ACIST

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·November 24, 2008

    TOSHIBA

    FDA Adverse Event
    Other ·TOSHIBA MEDICAL SYSTEMS CORP.·Product code LNH·April 2, 2009

    TOSHIBA

    FDA Adverse Event
    Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·December 4, 2012

    CANON CT SCANNER

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEMS USA, INC.·Product code JAK·November 30, 2018

    TOSHIBA

    FDA Adverse Event
    Injury ·TOSHIBA MEDICAL SYSTEM CORP·Product code ITX·April 15, 2009

    STERRAD 100S STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·April 12, 2010

    TOSHIBA

    FDA Adverse Event
    Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·March 11, 2011

    TOSHIBA

    FDA Adverse Event
    Death ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code KXJ·February 22, 2011

    Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device Listing Number: Dl53118. Diagnostic Ultrasound system.

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·April 24, 2013

    TOSHIBA

    FDA Adverse Event
    Malfunction ·TOSHIBA MEDICAL SYSTEMS·Product code IZI·December 29, 2003

    TOSHIBA X-SPEED

    FDA Adverse Event
    Malfunction ·TOSHIBA MEDICAL SYSTEMS·Product code JAK·November 11, 1994

    TOSHIBA AQUILON 64 CT SCANNER TABLE

    FDA Adverse Event
    Injury ·TOSHIBA MEDICAL SYSTEMS·Product code JAK·December 29, 2011

    TOSHIBA

    FDA Adverse Event
    Death ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·November 13, 2008

    TOSHIBA

    FDA Adverse Event
    Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·September 2, 2011

    TOSHIBA

    FDA Adverse Event
    Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·September 16, 2015

    TOSHIBA

    FDA Adverse Event
    Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·February 3, 2012

    AQUILION 16

    FDA Adverse Event
    Malfunction ·TOSHIBA AMERICA MEDICAL SYSTEMS·Product code JAK·February 19, 2009

    TOSHIBA

    FDA Adverse Event
    Malfunction ·TOSHIBA MEDICAL SYSTEMS CORP·Product code JAK·March 18, 2009