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

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    CT PROSPEED FAMILY

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPIVE NEEDLE SYSTEM, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CARE ELECTRIC BREAST PUMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SUPER MULTIVAC 50 WITH INTEGRATED CABLE

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code GEI·January 31, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·January 3, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 18, 2014

    DIMENSION EXL 200

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 23, 2013