BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    PHENCYCLIDINE EIA ASSAY

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867060104·ARTHREX ECLIPSE HUMERAL HEAD, 53/20

    RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    WLW

    FDA 510(k)
    FDA Class 2 ·Dental

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2013

    HOVEROUND CORPORATION

    FDA Adverse Event
    Injury ·HOVEROUND CORP.·Product code INI·December 16, 2010

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 15, 2014