BEUDAMED
    7 results · 17ms · 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.

    FILTERSET W/Y-INJECTION SITE, 0.2

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517822109·Interlock II Trial, 12x17x14mm 30° Stop

    CHEMISTRY CONTROL, ABNORMAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    eego amplifiers

    FDA 510(k)
    FDA Class 2 ·Neurology

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·October 2, 2012

    ACRYSOF RESTOR

    FDA Adverse Event
    Malfunction ·ALCON MANUFACTURING, LTD.·Product code HQL·December 18, 2013

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 23, 2010