BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Medcomp Vessel Dilator

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Z-BLOCK, MODELS 20/19, 40/19, 55/19

    FDA 510(k)
    FDA Class 2 ·Dental

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·February 14, 2013

    ASR ACETABULAR CUPS 58

    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