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

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    DOSI-FLOW, MODELS 20 & 30

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517701084·BASE Ti Implant, 8x38x28mm 10°

    SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DeVilbiss DV6WM Wireless Modem

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code DXY·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 23, 2014