BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    K032008

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code HXX·April 3, 2013

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·March 28, 2011

    LUMAX 340 VR-T

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code LWS·April 21, 2008