BEUDAMED
    19 results · 35ms · Sources: EU EUDAMED, US FDA

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    BORNING NEONATAL RESUSCITATOIN CENTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Fine Structure Analysis(fineSA)

    FDA 510(k)
    FDA Class 2 ·Radiology

    CUTERA FLASHLAMP TABLETOP AESTHETIC PRODUCT

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

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    DASHER -14 STEERABLE GUIDEWIRE

    FDA Adverse Event
    Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQX·January 9, 2007

    VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·June 4, 2014

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 26, 2012

    EXCELCARE BARIATRIC BED FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC·Product code FNL·September 28, 2010