BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    COJET SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00673978963099·INST 963-735 MAYFIELD CLAMP

    PRESYM TRCG TRACHEOCARDIOGRAM, MODEL 112

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SONGER(TM) CABLE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TROJAN PLEASURE PACK LUBRICATED CONDOMS

    FDA Adverse Event
    Injury ·CHURCH & DWIGHT CO., INC.·Product code HIS·October 29, 2014

    ACCOLADE 132 SIZE 4.5

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·February 15, 2013

    ICENTRAL

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE, FINLAND OY·Product code MSX·December 22, 2010

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 29, 2014