BEUDAMED
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    MEDEX 3000 SERIES SYRINGE INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301747·In-Situ Coronal Bender Tip, Left, 4.0mm

    LARGE AO COUPLING ASNIS III HALL FITTING

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 25, 2012

    VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM

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

    Powder Free Nitrile Examination Gloves (White, Cobalt Blue, Blue and Violet Blue)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    ADVIA CENTAUR CEA AND BR ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code DHX·June 27, 2008

    DIRECT DRIVE DISPOSABLE CLIP APPLIER 10MM 3/BOX

    FDA Adverse Event
    APPLIED MEDICAL·Product code GDO·February 25, 2013

    POLYHESIVE RETURN ELECTRODE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·January 13, 2011

    PLMA DVC V11.51 1 R

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 24, 2014