BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    UREA NITROGEN (BUN) LIQUI-UV

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Fresh Cells

    FDA UDI
    DIAGNOSTIC HYBRIDS, INC.·30014613334897·R-MIX CELLS MWP W24/18F

    Pioneer Plus Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K-SPRAY, MODEL 085-2715

    FDA 510(k)
    FDA Class 1 ·Dental

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 14, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·January 7, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014