BEUDAMED
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    MONOJECT(R) PISTON SYRINGES; 3,6,12,20,35 AND 60CC SIZES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ABL80 SC80

    FDA UDI
    Radiometer Medical ApS·05700699457158·SC80 200/30 BG/OX, QC3

    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    ACS ANGIOSCOPIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CINE RECALL FUNCTION/OPUS 1 REAL TIME SCANNER

    FDA 510(k)
    FDA Class 2 ·Radiology

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·November 29, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 6, 2013

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 4, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 21, 2014

    DURASUL, ALPHA INSERT, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·November 20, 2018