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

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    WALL IV EXTENSION TUBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IKNEE DISTAL FEMORAL CUTTING GUIDE

    FDA 510(k)
    FDA Class 2 ·Neurology

    EYE SPHERE IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CLEARVIEW UTERINE MANIPULATOR

    FDA Adverse Event
    Injury ·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 30, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·December 17, 2010

    PINNACLE 100 HA ACET CUP 60MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWA·July 17, 2014