BEUDAMED
    7 results · 18ms · 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.

    OMNIVIEW(TM) OPHTHALMIC FIBERENDO W/NEEDLEHOLDER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Malibu

    FDA UDI
    Seaspine Orthopedics Corporation·10889981081744·5.5mm, 6.5mm & 7.5mm Screw Caddy

    FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    WAVELENGTH MULTI-PURPOSE ULTRASOUND GEL

    FDA 510(k)
    FDA Class 2 ·Radiology

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code FSA·January 12, 2013

    INTEGRIS V3000

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZI·November 17, 2010

    INGENIO

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 3, 2014