BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    3M LVR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFIED CONCENTRIC MICROCATHETER, MODEL 90047

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OrthoGold

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013

    SIGMA 200 SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·February 15, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014