BEUDAMED
    7 results · 27ms · 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 ×

    BRANEMARK SYSTEM ZYGOMATICUS FIXTURE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970499·anteriors; shade BL2; mould BS

    PATIENT TURNING AND REPOSITIONING G DEV.

    FDA 510(k)
    FDA Class 1 ·General Hospital

    sensiLift

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 20, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT-722LNAS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·January 19, 2011

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014