BEUDAMED
    9 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.

    VERSABLADE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Kwik Kleen

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657016506·Kerrison 2mm x 200mm, 40 Deg

    Lip Bumper

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746073465·LIP BUMPER 045 DIA KIT OF 14

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981177690·6mm, 4-Hole Threaded Anterior Plate

    MILLER/NADLER GLARE TESTER

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    A-200 POWERED WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    FINELINE II

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·October 4, 2010

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 14, 2012