BEUDAMED
    14 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code FTL·October 16, 2012

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 3/12 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 5, 2024

    2520274-2013-04648

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code LRN·August 27, 2013

    OMEGA21 EXPANSIVE SCREW 7X35MM

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code MNI·November 22, 2013

    2520274-2013-10213

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·February 11, 2013

    PHASEAL INFUSION ADAPTER

    FDA Adverse Event
    Malfunction ·CARMEL PHARMA AB·Product code LHI·February 1, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 20, 2008

    CATALYS SYSTEM

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING USA, LLC·Product code OOE·August 15, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING NETHERLANDS·Product code MFK·August 5, 2025

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·August 2, 2011

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 30, 2023

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 30, 2023

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 30, 2023

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 1, 2021