BEUDAMED
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    3M AURORA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295251149·SIGMA CURVED PLUS INSERT TRIAL SIZE 3 20mm

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707035280·.017 X .025 Lower Elastinol™ Standard Form Arch...

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111116·KATENA INSTRUMENT RACK

    BLOOD LINE COMP. NEG. PRESS. PILLOW

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OSSIFUSE BONE SUBSTITUTE MATERIAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DATASCOPE MR MONITOR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP./PT MONITORING DIVISION·Product code MHX·January 23, 2003

    IMUFLEX DISPOSBLES

    FDA Adverse Event
    Malfunction ·TERUMO BCT·Product code KSR·February 21, 2013

    REGIONAL ANALGESIA INFUSOR W/PATIENT CONTROL MODULE 5.0-7.0

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 28, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014