BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    NON-STERILE E.P. LATEX EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    4CIS SOLAR AND APOLLON SPINE SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ICOONE h (also referred to as ICOONE LASER and ICOONE –h LASER)

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

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 28, 2013

    UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LFX·February 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014