BEUDAMED
    5 results · 26ms · 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 × Regulation: Us FDA × Clear all

    AEYE-DS RETINA SCREENING

    FDA Adverse Event
    Injury ·AEYE HEALTH INC.·Product code PIB·January 22, 2025

    AMPLATZER TALISMAN PFO OCCLUDER

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code MLV·November 22, 2022

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·August 17, 2011

    *

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code IZI·July 18, 2008

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, NEUROMODULATION·Product code LGW·July 9, 2013