BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    FOUR-CHANNEL PREAMPLIFIER

    FDA 510(k)
    FDA Class 2 ·Neurology

    Humelock Reversed Shoulder

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PHILIPS ADULT REUSABLE SP02 SENSOR, MODEL M1191B, M1191BL, M1191BNL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SIMPLEX TOBRAMYCIN 1 PK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·February 14, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    UNKNOWN·Product code IKX·July 29, 2014

    OT SURESTEP METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·December 6, 2010