BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SNAP-RING FOR 52MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 4, 2007

    TYPE7B

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·May 27, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 7, 2013

    COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, IRVINE·Product code OAD·October 22, 2010

    SPINALPAK ASSEMBLY

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·October 30, 2020

    BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·October 25, 2023

    SPINALPAK ASSEMBLY

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·March 22, 2021