BEUDAMED
    8 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SELOX SR 53

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code LWS·June 14, 2006

    HERAEUS MEDICAL PALACOS R+G BONE CEMENT

    FDA Adverse Event
    Injury ·.·Product code JWH·November 1, 2016

    SPIROFLEX® ANGIOJET® THROMBECTOMY SET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DXE·August 17, 2016

    PALACOS R 1X40 SINGLE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LOD·May 9, 2017

    TI PEDICLE HOOK/DUAL-OPENING SIDE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code KWP·February 8, 2013

    FIBER ONE

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER-SILICON VALLEY·Product code GEX·December 7, 2010

    CAPTURE-R SELECT

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSS·July 22, 2014

    NEXGEN MIS STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·October 4, 2016