BEUDAMED
    23 results · 64ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MOLIFT QUICKRAISER 205 ACTIVE

    FDA Adverse Event
    Malfunction ·ETAC A/S·Product code FSA·January 22, 2024

    MOLIFT

    FDA Adverse Event
    Malfunction ·ETAC A/S·Product code FSA·July 14, 2022

    AMPUTEE LEGREST FOR ETAC WHEELCHAIR CROSS

    FDA Adverse Event
    Injury ·ETAC SUPPLY CENTER AB·Product code INM·November 12, 2012

    MOLIFT MOVER 180

    FDA Adverse Event
    Malfunction ·ETAC AS (DIVISION ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·March 11, 2014

    MOLIFT SMART 150

    FDA Adverse Event
    Malfunction ·ETAC AS (DIVISION ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·May 21, 2013

    MOLIFT SMART 150

    FDA Adverse Event
    Malfunction ·ETAC AS (DIVISIION ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·May 21, 2013

    MOLIFT SMART

    FDA Adverse Event
    Other ·ETAC AS (DIV ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·May 22, 2013

    MOLIFT SMART 150

    FDA Adverse Event
    Malfunction ·ETAC AS (DIVISION ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·May 21, 2013

    MOLIFT SMART

    FDA Adverse Event
    Other ·ETAC AS (DIV ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·May 22, 2013

    MOLIFT SMART

    FDA Adverse Event
    Other ·ETAC AS (DIV ETAC SUPPLY GJOEVIK, NORWAY)·Product code FSA·May 22, 2013

    MOLIFT SMART

    FDA Adverse Event
    Death ·ETAC AS (DIVISION ETAC SUPPLY GJOVIK, NORWAY)·Product code FSA·May 21, 2013

    MOLIFT MOVER 180

    FDA Adverse Event
    Malfunction ·ETAC AS (DIVISION ETAC SUPPLY GJOEVIK, NORWAY·Product code FSA·December 6, 2013

    MOLIFT MOVER 180

    FDA Adverse Event
    Malfunction ·ETAC AS (DIVISION ETAC SUPPLY GJOEVIK, NORWAY·Product code FSA·December 12, 2013

    TARGET HELICAL ULTRA 3MM X 8CM

    FDA Adverse Event
    Death ·STRYKER NEUROVASCULAR CORK·Product code HCG·June 7, 2022

    DIMENSION®

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code MLM·May 17, 2019

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code NJE·May 9, 2018

    GALAXY G3 XSFT 2.5MM X 3.5CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·October 23, 2019

    NEUROFORM ATLAS 3.0MM X 15MM NO TIP - CE

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code NJE·March 17, 2023

    XTRASOFT ORBIT GALAXY DETACHABLE COIL

    FDA Adverse Event
    CODMAN AND SHURTLEFF, INC·Product code HCG·August 19, 2015

    EVIS EXERA III XENON LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·October 7, 2022