BEUDAMED
    9 results · 17ms · 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 Status: Malfunction ×

    LEAD APRON

    FDA Adverse Event
    Malfunction ·BURLINGTON MEDICAL SUPPLIES·Product code EAJ·July 25, 1997

    MAGNESIUM

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code JGJ·December 21, 2020

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·October 19, 2016

    MEDEX TRANSTAR KITS

    FDA Adverse Event
    Malfunction ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code DPT·May 15, 2025

    KLF-001-600 .6MM FIBER

    FDA Adverse Event
    Malfunction ·OPTICAL INTEGRITY·Product code GEX·June 7, 2023

    ACCOLADE EL DR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWP·September 11, 2018

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 12, 2014

    PORTEX BLUE LINE ULTRA FENESTRATED INNER CANNULA TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL CZECH REPUBLIC A. S·Product code BTO·April 22, 2025

    SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 3, 2019