BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    ACU-TEST IN-HOME PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Spectra Optia Apheresis System

    FDA 510(k)
    FDA Unclassified ·Unknown

    FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 30, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 10, 2012

    ACCU-CHEK INFORM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·July 25, 2007