BEUDAMED
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    ENDOSCOPE STERILIZATION TRAY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SimplyGo Mini

    FDA UDI
    Respironics, Inc.·00606959047433·SimplyGo Mini Device, Japan

    EVACUATED CONTAINER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code GCY·January 25, 2019

    STRYKER IVAS BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THERMAGE THERMACOOL SYSTEM

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

    VITEK® 2 AST-YS08 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code NGZ·January 11, 2018

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION COROPORATION·Product code FPA·May 1, 2013

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 2, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 20, 2011