BEUDAMED
    149 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FLEXABS ELECTRICAL MUSCLE STIMULATION DEVICE

    FDA Adverse Event
    Malfunction ·JKH HEALTH CO., LTD.·Product code NGX·July 25, 2024

    FLEXABS ELECTRICAL MUSCLE STIMULATION DEVICE

    FDA Adverse Event
    Malfunction ·JKH HEALTH CO., LTD.·Product code NGX·July 25, 2024

    FLEXABS ELECTRICAL MUSCLE STIMULATION DEVICE

    FDA Adverse Event
    Malfunction ·JKH HEALTH CO., LTD.·Product code NGX·July 25, 2024

    FLEXABS

    FDA Adverse Event
    Malfunction ·JKH HEALTH CO., LTD.·Product code NGX·May 9, 2024

    FLEXABS

    FDA Adverse Event
    Malfunction ·JKH HEALTH CO, LTD.·Product code NGX·October 7, 2024

    VIVERITY

    FDA Adverse Event
    Injury ·JKH HEALTH CO., LTD.·Product code GZJ·August 21, 2017

    VIVERITY

    FDA Adverse Event
    Injury ·JKH HEALTH CO., LTD.·Product code GZJ·August 21, 2017

    UNK

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·January 26, 2009

    SMARTTOUCH

    FDA Adverse Event
    Malfunction ·MICROPORT CRM S.R.L.·Product code MRM·April 17, 2024

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·March 21, 2012

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·June 3, 2014

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·June 7, 2012

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·July 30, 2014

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·October 29, 2014

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·July 2, 2012

    NEUROTHERM JK3

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code GXD·January 5, 2018

    NEUROTHERM JK3

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·June 14, 2018

    ANTI-JKA

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·June 30, 2015

    EMERSON DISPOSABLE DRAINAGE UNIT

    FDA Adverse Event
    Malfunction ·J.H. EMERSON COMPANY·Product code EYZ·June 30, 1992

    EMERSON

    FDA Adverse Event
    Malfunction ·J.H. EMERSON CO.·Product code KDQ·April 28, 2004