BEUDAMED
    9 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TUFF UNICON IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 23, 2026

    TUFF UNICON IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 23, 2026

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 11, 2014

    TUFF UNICON IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·June 18, 2025

    2520274-2013-01419

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 13, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·February 25, 2011

    GE OEC 6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 22, 2008

    COUPLER AC ZOOM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code FEM·October 14, 2021

    SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·February 17, 2021