BEUDAMED
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    HOUTS HYSTERECTOMY DRAIN

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197775·AK3 PS-C Insert Trial Size 2, 20mm

    ARIES MEDICAL PERFLEX PERCUTANEOUS 40CC D/L BALLOO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HYBRID PERIPHERAL DILATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AT HOME DRUG TEST PHARATECH

    FDA Adverse Event
    PHAMATECH·Product code MVO·September 24, 2003

    STOCKERT CENTRIFUGAL PUMP CONSOLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·June 17, 2014

    T4/WD2418/HD/ADULT/28/BH16/AT903/U2222C/COM/U550 9153639569

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·July 7, 2015

    SPACEMAKER BLUNT TIP TROCAR 10MM

    FDA Adverse Event
    Malfunction ·USSC PUERTO RICO·Product code GCJ·November 3, 2010

    VANGUARD COMPLETE KNEE SYSTEM XP-XP TIBIAL TRAY 67MM ¿ INTERLOK LOCKING BAR & CE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·December 1, 2016