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

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    BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    H.R. JAKOBI SURG. INSTRUMENTS #11 38/67

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB

    FDA 510(k)
    FDA Class 2 ·Radiology

    M-PORT SI INJECTOR

    FDA Adverse Event
    Injury ·BAUSCH & LOMB INCORPORATED·Product code MSS·July 1, 2015

    1/4" SQUARE 4MM DRIVER

    FDA Adverse Event
    Malfunction ·SEASPINE, INC.·Product code KWQ·February 6, 2014

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·December 27, 2012