BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    iMAR

    FDA 510(k)
    FDA Class 2 ·Radiology

    OPUS MINIMAGNUM ANCHOR WITH INSERTER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMC HYPODERMIC NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 2, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 5, 2025

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2018

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·June 3, 2013

    AFFINITY 4

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code HDD·June 21, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008