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

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    OHMEDA AUXILIARY POWER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Legacy™3 Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307102380·3.2mmD x 8mmL, 3.0mmD Platform

    Shoreline™ ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981143916·Trial Rasp, 18x15x8mm, 7 Deg Lordosis

    MAGNESIUM ASSAY (XB), MODELS 125-12, 125-50 AND 125-S7

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SIRECUST 358

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPSUREFIX NOVUS

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

    VIRTUOSO DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·October 9, 2010

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·December 10, 2012