BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    INSTRUMENT STERILIZATION TRAY

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

    SPECTRON CONVERSION ENDOPROSTHESIS CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLC SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 10, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·October 11, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 10, 2012

    AIM-ARM F/LFN

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code LXH·July 11, 2016

    AIMING ARM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code LXH·July 13, 2016

    STANDARD INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code LXH·July 11, 2016