BEUDAMED
    3,384 results · 24ms · Sources: EU EUDAMED, US FDA

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    KXO-80G

    FDA 510(k)
    FDA Class 1 ·Radiology

    KXO-80C/80D

    FDA 510(k)
    FDA Class 1 ·Radiology

    X-RAY GENERATOR MODEL KXO-15

    FDA 510(k)
    FDA Class 1 ·Radiology

    KALARE DIAGNOSTIC X-RAY SYSTEM KXO-80XD

    FDA Adverse Event
    Injury ·TOSHIBA·Product code JAA·October 29, 2013

    X-Ray High Voltage Generator, Model KXO-80G used on Image Intensified Fluoroscopoc X-Ray System DUA-450D

    FDA Recall
    Terminated ·Toshiba American Med Sys Inc·Product code rad·September 7, 2004

    Toshiba Ultimax DREX-ULT80 X-ray generator

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·March 22, 2017

    Toshiba Kalare DREX-KL80 X-ray generator

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·March 22, 2017

    INTRAN PLUS IUP-400

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS INC.·Product code KXO·February 25, 2009

    INTRAN PLUS

    FDA Adverse Event
    Death ·UTAH MEDICAL PRODUCTS, INC.·Product code KXO·August 2, 1996

    INTRAN PLUS

    FDA Adverse Event
    Death ·UTAH MED PRODUCTS, INC.·Product code KXO·September 6, 1996

    INTRAN PLUS

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code KXO·August 2, 1996

    HUAM UTERINE ACTIVITY MONITOR

    FDA Adverse Event
    Malfunction ·CORAM HEALTHCARE CORP.·Product code KXO·April 17, 1996

    INTRANPLUS IUP-C50

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS·Product code KXO·October 9, 2008

    ACCU-TRACE IUPC INTRAUTERINE PRESSURE CATHETER

    FDA Adverse Event
    Malfunction ·KENDALL·Product code KXO·September 19, 2011

    4000 SOFTRANS IUPC

    FDA Adverse Event
    Malfunction ·KENDALL LTP·Product code KXO·October 2, 2000

    1718873-1997-00001

    FDA Adverse Event
    Injury ·Product code KXO·August 14, 1997

    KOALA

    FDA Adverse Event
    Injury ·CLINICAL INNOVATIONS, INC·Product code KXO·September 24, 1997

    KOALA

    FDA Adverse Event
    Injury ·CLINICAL INNOVATIONS, INC.·Product code KXO·September 24, 1997

    QWIK CONNECT SPIRAL

    FDA Adverse Event
    Other ·COROMETRICS·Product code KXO·August 31, 1998

    INTRAN PLUS IUP-400

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code KXO·December 18, 2008