BEUDAMED
    8 results · 19ms · 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 ×

    BAYLIS MEDICAL RF SEPTOSTOMY GENERATOR, NYKANEN RF SEPTOSTOMY CATHETER, BAYLIS MEDICAL CONNECTOR CABLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RES-Q INFANT WEDGE AND SLING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Bengal Stackable Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EQUINOXE CAGE GLENOID LARGE, BETA

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·July 2, 2024

    OPEN SPINE ANGLED CLAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·June 14, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 5, 2013

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 7, 2014