BEUDAMED
    9 results · 20ms · 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.

    BACKSTOP CATHETER, MODEL 60-0000-3100

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036028305·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450223826·

    ELECSYS CORTISOL TEST SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    TREMOROMETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    PREMILENE 0 (3.5) 75CM DS30 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAW·May 12, 2016

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 2, 2013

    VITROS CHEMISTRY PRODUCTS GLU SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code CGA·September 15, 2014

    THORATEC PVAD

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·May 16, 2011