BEUDAMED
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    PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CPI

    FDA Adverse Event
    Injury ·CPI--CARDIAC PACEMAKER, INC.·Product code DXY·June 12, 1997

    MODEL 3500 MR-COMPATIBLE PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CATHETER INTRODUCER MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·August 1, 2014