BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    MN-111

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Orbit Depressor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100912·SCHOCKET SCLERAL DEPRESSOR

    BLOOD PRESSURE CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FINGERTIP PULSE OXIMETER, MODEL MD300I

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISCOVERY

    FDA Adverse Event
    Injury ·GUIDANT CLONMEL IRELAND·Product code NVZ·July 22, 2011

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 31, 2013

    INVACARE RELIANT 450

    FDA Adverse Event
    Injury ·INVACARE LINAK U.S. INC.·Product code FSA·July 25, 2008