BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    SILVERLON BURN CONTACT DRESSINGS

    FDA 510(k)
    FDA Unclassified ·Unknown

    Oticon

    FDA UDI
    Oticon A/S·05707131287267·RIA2 PRO, MINIRITE 312 WL SIL

    IRIS Anterior Cervical Plate System

    FDA UDI
    Life Spine, Inc.·00190837060787·Iris Screw Removal Sleeve

    Tray Pin 3+

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215074036·

    THE IC-PRO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTOR

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    IHEARTEST

    FDA Adverse Event
    Malfunction ·IHEAR MEDICAL, INC.·Product code EWO·August 17, 2022

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 29, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 10, 2011

    ROTALINK CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code MCX·September 3, 2008

    MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021