BEUDAMED
    6 results · 26ms · 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.

    CARAPACE SUTURE REMOVAL TRAYS

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DIO-DENT 10 DENTAL DIODE LASER

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

    PC ECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code KQS·November 30, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 28, 2013

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·July 14, 2014