BEUDAMED
    4 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC., USA·Product code LFR·October 16, 2007

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FZW·October 18, 2012

    ALARIS® PCA MODULE

    FDA Adverse Event
    Death ·CAREFUSION·Product code FRN·October 23, 2018