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

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    MODIFIED LABEL TO PERCU. INTRO. W/SIDEPORT & 3-WAY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756588287·MP-317771 CUSTOM AMNIO TRAY

    RIGIDENT CREAM

    FDA 510(k)
    FDA Class 1 ·Dental

    OMNI INFANT PHOTOTHERAPY UNIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GEMSTAR PM PMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 25, 2014

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KPE·January 3, 2013

    MAXIM POS FEMORAL AUGMENT BOLT 75 X 10MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·November 9, 2010