BEUDAMED
    58 results · 20ms · Sources: EU EUDAMED, US FDA

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    ARTHREX TAK FAMILY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024

    BD PHOENIX SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 6, 2021

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 8, 2024

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2024

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    RHIGENE MESACUP2 TEST- SSA

    FDA 510(k)
    FDA Class 2 ·Immunology

    ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VPV SYSTEM

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF MEDOS·Product code JXG·January 6, 2014

    CODMAN VIPV SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC. MEDOS S.A.·Product code JXG·November 5, 2010

    CODMAN VPV SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·January 11, 2018

    CODMAN VPV SYSTEM

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·October 1, 2016