BEUDAMED
    6 results · 29ms · 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 ×

    A&E MEDICAL CORP DISPOS SUCT COAG W/NON STICK COAT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    FLOCARE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    LIFESIGN DOA 4 (THC/OPI/COC/MET)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    GROSHONG NXT CLEARVUE 4 FR SINGLE LUMEN, FULL TRAY WITH MI

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code LJS·December 1, 2010

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·REPIRONICS CALIFORNIA INC·Product code MNT·July 3, 2014

    HEARTSTART XL + DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 7, 2012