BEUDAMED
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    IN VITRO TEST DETERMINATION OF INORGANIC PHOSPHORO

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209126842·

    JAKOBI SURG. INSTRUMENTS #7 10/43

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Meniscus Versaflex

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

    TRI-LOCK BPS SZ 1 STD OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code KWA·June 6, 2014

    MONARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·November 29, 2012

    COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, IRVINE·Product code OAD·September 3, 2010