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

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    COROENT XL-F SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131270290·H11, DESIGNRITE 10 WL TC

    PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PEDIATRIC ENERGY REDUCER, MODELS AED-10 AND AED-20

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    AEQ REVERSED II GLENOID SPHERE D.42MM CENTER D 25MMBASEPLATE

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·October 2, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2025

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 31, 2013

    PROTECTIV SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code FOZ·June 23, 2011

    INOGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 3, 2014

    AEQ REV II GLENOID BASEPLATE DIA 25MM LONG POST

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·January 7, 2025