BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    NEPHELRATE ANTISERUMS 1GA

    FDA 510(k)
    FDA Class 2 ·Immunology

    Renovis S180 Lateral Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES (LIGHT YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    METRX® SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·January 9, 2025

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·April 30, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·October 11, 2012

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·August 3, 2010