BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    TYCOS DIAGNOSTIC PENLIGHT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Gexfix External Fixation

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KEDALL 14.5 FR CHRONIC HEMODIALYSIS CATHETER W/SILVER IMPREGNATED SLEEVE (PALINDROME RUBY)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UNKNOWN

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DQY·April 11, 2014

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 17, 2007

    LIGHTWAVE SUCTION ABLATOR

    FDA Adverse Event
    Injury ·CONMED LINVATEC·Product code GEI·September 26, 2012