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

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    DIRECT VIEW 2001 FIBERLIGHT

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    KINEMAX(R) CONDYLAR TOTAL KNEE SYST FEMORAL SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NON-WOVEN SPONGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    PROSTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code KNS·February 6, 2013

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·December 28, 2010

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 21, 2014