BEUDAMED
    6 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.

    BIOPSY NEEDLE GUIDE ATTACHMENT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LIGHT CURED RESIN BONDED CERAMIC

    FDA 510(k)
    FDA Class 2 ·Dental

    GEODESIC EEG SYSTEM 300

    FDA 510(k)
    FDA Class 2 ·Neurology

    RX90-2 ARCOM HW/32MM LINER SZ 44

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·June 10, 2014

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·October 11, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012