BEUDAMED
    13 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ANDAGO

    FDA Adverse Event
    Malfunction ·HOCOMA AG·Product code BXB·December 22, 2017

    LOKOMAT PRO

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code IKK·November 30, 2017

    LOKOMAT-SYSTEM

    FDA Adverse Event
    Malfunction ·HOCOMA AG·Product code ISD·April 27, 2005

    LOKOMAT SYSTEM

    FDA Adverse Event
    Malfunction ·HOCOMA AG·Product code BXB·May 29, 2009

    LOKOMATPRO

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code IKK·May 20, 2022

    LOKOMATPRO

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code BXB·July 18, 2025

    LOKOMATPRO

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code IKK·April 21, 2023

    LOKOMAT-SYSTEM

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code ISD·November 5, 2004

    LOKOMAT

    FDA Adverse Event
    Malfunction ·HOCOMA AG·Product code IKK·January 28, 2019

    HOCOMA

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code BXB·May 28, 2026

    LOKOMATPRO

    FDA Adverse Event
    Malfunction ·HOCOMA AG·Product code IKK·January 28, 2020

    LOKOMAT

    FDA Adverse Event
    Injury ·HOCOMA AG·Product code IKK·December 4, 2019

    LOKOMATPRO

    FDA Adverse Event
    Malfunction ·REGULATORY INSIGHT, INC. (HOCOMA AG)·Product code IKK·August 3, 2016