BEUDAMED
    58 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPES MEDICA SUBDERMAL NEEDLE ELECTRODES

    FDA Adverse Event
    Malfunction ·SPES MEDICA SPA·Product code GXZ·December 15, 2025

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMF·April 9, 2024

    RADIESSE

    FDA Adverse Event
    Injury ·BIOFORM MEDICAL, INC.·Product code LMH·December 15, 2007

    RADIESSE DERMAL FILLERS

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 29, 2024

    RADIESSE DERMAL FILLERS

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 29, 2024

    RADIESSE DERMAL FILLERS

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 29, 2024

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC·Product code FMF·April 27, 2023

    SCULPTRA

    FDA Adverse Event
    Injury ·GALDERMA LABORATORIES, L.P.·Product code LMH·July 29, 2024

    COOLSCULPTING

    FDA Adverse Event
    Injury ·ALLERGAN / ZELTIQ AESTHETICS INC.·Product code OOK·February 2, 2024

    BELLAFILL

    FDA Adverse Event
    Injury ·SUNEVA·Product code LMH·January 28, 2016

    AB MEDICA CURVED SCISSOR AND INSERT

    FDA Adverse Event
    Malfunction ·AB MEDICA SAS·Product code GCJ·June 23, 2022

    MICROLAP INSULTATED OUTER TUBE

    FDA Adverse Event
    Malfunction ·AB MEDICA SAS·Product code GCJ·December 5, 2018

    OUTER TUBE

    FDA Adverse Event
    Injury ·AB MEDICA SAS·Product code GCJ·March 23, 2020

    LOW IMP FENES GRSP FRCP JAW IN

    FDA Adverse Event
    Malfunction ·AB MEDICA SAS·Product code GCJ·May 29, 2018

    MICROLAP CRVD SCISSORS INSERT

    FDA Adverse Event
    Injury ·AB MEDICA SAS·Product code GCJ·August 27, 2019

    BELOTERO

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·May 1, 2019

    HYDROGEL

    FDA Adverse Event
    Injury ·UNK·Product code PFP·November 24, 2020

    MORPHEUS 8 RADIO FREQUENCY DEVICE

    FDA Adverse Event
    Injury ·INMODE LTD.·Product code GEI·October 21, 2025

    SYLFIRM X

    FDA Adverse Event
    Injury ·BENEV / VIOL CO., LTD.·Product code GEI·June 13, 2023

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Injury ·RH-USA·Product code GEX·November 2, 2007