BEUDAMED
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    LASER RESISTANT TRACHEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MYOTEST DBS NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM

    FDA 510(k)

    VerSys® Hip System

    FDA UDI
    Zimmer, Inc.·00889024143937·

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 26, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·January 4, 2013

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 11, 2010

    HEARTMATE 3 SEALED OUTFLOW GRAFT WITH BEND RELIEF

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·August 30, 2023