BEUDAMED
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    STERILE EXTENSION TUBES INDIV. PKG.

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO: PSS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sutter Arrowtip Monopolar Electrodes

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 8, 2014

    M2A-MAGNUM MOD HD SZ 56MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 16, 2012

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·May 22, 2015