BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    No-contact Forehead Thermometer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PETERIO UNIVERSAL LASER SCANNING HANDPIECE

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

    MAXLOCK EXTREME SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PAINSMART

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 30, 2013

    OPTI-FIX

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, ORTHOPEDICS·Product code JDH·July 23, 2011

    UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·September 19, 2008