BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300

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

    6893491

    FDA Adverse Event
    Malfunction ·September 26, 2017

    HIP SEXTANT INSTRUMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    restor3d Metallic Interference Screw

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFESHIELD PRIMARY SYMBIQ SET PIGGYBACK WITH BACK CHECK VALV

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FPK·June 13, 2014

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 2, 2013

    ENSEAL TRIO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY·Product code GEI·October 12, 2010