BEUDAMED
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    UROLOGICAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    IntelliVue Patient Monitor MX500, IntelliVue Patient Monitor MX550

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SORB SYSTEM URS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EQUALIZER OCCLUSION BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQY·March 1, 2013

    OXFORD UNICOMPARTMENTAL KNEE PHASE 3 TIBIAL TRAY WIDE 41 X 26MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014