BEUDAMED
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    ATRAUMATIC STANDARD SPROTTE NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PAQ.112X90X300.SUZ-KENZ

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763008613·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704260069·

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756020176·FINGER SPLINT

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G5869112020·round caps, gas or steam permeable, can be used...

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112020·Tap, 4.75 mm

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0112020·Tap, 4.75mm

    SURGICAL TISSUE MANAGEMENT SYSTEM

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

    MSI BIPOLAR SHEATH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 11, 2013

    6464602R PCA II PUMP REFUBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - ANDOVER·Product code FRN·November 30, 2010

    TECNIS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·July 2, 2014