BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    FIAX(R) TEST KIT CYTOMEGALOVIRUS M ANTIBODIES

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION KIT, MODEL 01-080000

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OPTIMA MDT PULSE GENERATOR W/TELEMETRY

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 10, 2014

    CARDIFIX

    FDA Adverse Event
    Malfunction ·GUIDANT ANGLETON/ST. PAUL·Product code NVN·October 11, 2010

    2520274-2012-03655

    FDA Adverse Event
    Injury ·SYNTHES·Product code HRS·December 10, 2012