BEUDAMED
    14 results · 22ms · 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 ×

    LIGACLIP MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·LACEY MANUFACTURING CO·Product code GDO·July 28, 2000

    SMR REVERSE HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022

    SMR GLENOSPHERE Ø 40MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·December 15, 2021

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·December 22, 2025

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 8, 2013

    BIVONA TTS CUFFED PEDIATRIC TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JOH·February 17, 2011

    LIKO

    FDA Adverse Event
    Injury ·LIKO NORTH AMERICA·Product code FSA·February 12, 2008

    PRIMEADVANCED

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LGW·July 22, 2016

    POWERLED TM

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·February 5, 2026

    RUMI II KOH-EFFICIENT

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·August 7, 2024

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·November 7, 2023

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 12, 2018

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 3, 2025

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 3, 2025