BEUDAMED
    11 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    POST-OP KNEE ORTHOSIS

    FDA Adverse Event
    Malfunction ·CORFLEX·Product code ITQ·May 20, 2022

    UNIVERSAL KNEE IMMOBILIZER

    FDA Adverse Event
    CORFLEX·Product code IQI·December 9, 2010

    AMBU PERFIT COLLAR

    FDA Adverse Event
    Malfunction ·CORFLEX·Product code IQK·September 24, 2018

    CE RIGHT HAND SPLINT

    FDA Adverse Event
    Injury ·CORFLEX·Product code IQI·January 23, 2018

    CORFLEX KNEE IMMOBILIZERS

    FDA Adverse Event
    CORFLEX UNIVERSAL·Product code IQI·December 3, 2012

    AORFLEX DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·LOMBARD MEDICAL·Product code MIH·February 13, 2015

    DIMENSION VISTA®

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code CHN·March 1, 2017

    MARATHON

    FDA Adverse Event
    Injury ·COREFLEX·Product code ITQ·July 26, 2005

    COFLEX

    FDA Adverse Event
    Injury ·COFLEX·Product code NQO·August 12, 2023

    PSORALITE COM FLEX JOULEE 4.1

    FDA Adverse Event
    Injury ·PSORALITE CORPORATION·Product code KGL·March 26, 1992

    PSORALITE COM FLEX JOULEE 4.1

    FDA Adverse Event
    Injury ·PSORALITE CORPORATION·Product code FTC·July 30, 1992