BEUDAMED
    9 results · 23ms · 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 Regulation: Us FDA ×

    Liberty SI Lateral Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JDEVOLUTION S

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·August 6, 2025

    ULTRASITE VALVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEURODYN PORTABLE TENS NFES, NEURODYN PORTABLE TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    GORE HELEX SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MLV·November 13, 2008

    FOLFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·September 1, 2011

    PELVICOL 2X4 CM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code FTL·July 11, 2013

    BD AUTOSHIELD DUO PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 6, 2020

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code MEA·July 3, 2023