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

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    MADSEN ACCUSCREEN TYPE 1077

    FDA 510(k)
    FDA Class 2 ·Neurology

    HI-TORQUE POWERTURN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CUTTING EDGE SPINE INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 14, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 7, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·February 7, 2012

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 23, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    UNKNOWN·Product code IKX·October 1, 2014

    CODMAN EXTERNAL DRAINAGE SYSTEM III

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·May 29, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 2, 2026

    ULTRAFLEX DUO CART WITH SMOKE EVAC

    FDA Adverse Event
    Malfunction ·DORNOCH·Product code JCX·September 13, 2018