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

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    Navigated Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    LANDANGER

    FDA UDI
    LANDANGER·03661219432777·

    BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304254244·

    MEDICALGORITHMICS UNIFIED ARRHYTHMIA DIAGNOSTIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOSCOPIC MONOPOLAR INSTRUMENTS AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD VENFLON¿ PERIPHERAL PORTED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·June 7, 2022

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 11, 2013