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

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    SKYTRON EXAM LIGHT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO NAUTILUS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER FREE LATEX SURGEONS GLOVES POLYMER COATED STERILE WITH OPTIONAL LABELING CLAIM OF E.P. LESS THAN 50 UG/DM2

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

    SM204-M-SERIES W/BIG WHELL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·December 21, 2012

    HEMOFILTRATION UNIT BM11 + BM14

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES GERMANY GMBH·Product code KDI·December 20, 2010

    COULTER ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 15, 2014