BEUDAMED
    8 results · 25ms · 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.

    WH150 ROOM HUMIDIFIER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G586N8716610·loute wire tightener, 8 1/2" (22.0 cm)

    ALPHAONE BIOFEEDBACK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Scopis Extended Instrument Set EM

    FDA 510(k)
    FDA Class 2 ·Neurology

    ALLURA XPER FD20

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·April 16, 2014

    PULSAR MAX

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·October 15, 2010

    THERAPY COOL FLEX, 1304-CF-7-0.5(5)2-L1-TE4BE1BE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-IRVINE)·Product code OAD·December 11, 2012

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026