BEUDAMED
    82 results · 16ms · Sources: EU EUDAMED, US FDA

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    TEG 6S HEMOSTASIS SYSTEM CITRATED K, KH, RT, FF

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORPORATION·Product code JPA·December 9, 2022

    KGH ROBOTIC PACK

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code LRO·November 5, 2020

    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

    KCH FETAL BLADDER DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·ROCKET MEDICAL PLC·Product code KOD·May 15, 1997

    ROCKET KCH FETAL BLADDER DRAIN

    FDA Adverse Event
    Malfunction ·ROCKET MEDICAL PLC·Product code MPR·November 19, 2020

    LENSAR LASER SYSTEM-FS 3D

    FDA Adverse Event
    Injury ·LENSAR, INC·Product code OOE·June 28, 2022

    LT 270-54, EASYPUMP, 270 ML, 5 ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code MEB·November 7, 2012

    COMPLETE MOISTUREPLUS

    FDA Adverse Event
    Injury ·ADVANCED MEDICAL OPTICS, INC.·Product code LPN·July 3, 2007

    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

    ALWAYS MAXI PAD WITH FLEXI-WINGS, OVERNIGHT EXTRA HEAVY (NOT

    FDA Adverse Event
    Injury ·KNH ENTERPRISE CO. LTD·Product code HHD·October 30, 2009

    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

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2022

    THE KOH COLPOTOMIZER SYSTEM

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL - THE KOH COLPOTOMIZER SYSTEM·Product code HEW·February 7, 2011