BEUDAMED
    40 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 9, 2024

    TORNIER FLEX SHOULDER SYS REVINSERT 42MM 9TH B 12.5DG

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·August 14, 2024

    AEQUALIS REVERSED GLENOSPHERE LAT.4 42MM X 25MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·August 14, 2024

    TORNIER HRS PTC PARTIALLY COATED DISTAL STEM DIA 15X90

    FDA Adverse Event
    Injury ·TORNIER INC·Product code KWS·August 14, 2024

    TORNIER HRS SPACER 15MM DIA 20MM LENGTH

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·August 14, 2024

    TORNIER FLEX SHOULDER SYS REV TRAY 0TH 0MM OFFSET

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·August 14, 2024

    AEQ REVERSED II GLENOID BASE PLATE DIA 25MM TYPE PLOT LONG

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·August 14, 2024

    SYNVISC ONE

    FDA Adverse Event
    Injury ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·December 27, 2018

    UNKNOWN HRS ASSEMBLY SCREW

    FDA Adverse Event
    Injury ·TORNIER INC·Product code KWS·August 14, 2024

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 16, 2014

    PROGRIP

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·August 11, 2020

    PROGRIP

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·August 11, 2020

    SYSMEX XN-10

    FDA Adverse Event
    Injury ·SYSMEX CORPORATION, I SQUARE·Product code GKZ·August 18, 2023

    TORNIER HRS PROXIMAL BODY DIA 15

    FDA Adverse Event
    Injury ·TORNIER INC·Product code KWS·August 14, 2024

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·May 12, 2005

    ULTREX

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FHW·August 27, 1997

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code NPT·October 27, 2017

    UNICEL DXH 900 COULTER CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code GKZ·January 27, 2026

    COULTER® ACT DIFF 2? ANALYZER

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code GKZ·November 26, 2013