BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    Ceribell Pocket EEG Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    ULTRA DCI MODEL 5000

    FDA 510(k)
    FDA Class 2 ·Radiology

    FETCH ASPIRATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POLYFORM SYNTHETIC MESH

    FDA Adverse Event
    Injury ·PROXY BIOMEDICAL LTD.·Product code FTL·June 4, 2013

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 20, 2011

    PROXIMATE RELOADABLE LINEAR STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 12, 2008