BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    U2 Total Knee System – PF+ Patella; USTAR II System– PF+ Patella

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BAND-AID BRAND SHEER COMFORT FLEX BAN

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER COMPANIES, INC.·Product code KGX·February 23, 2007

    Non-Contact Forehead Thermometer (UT30H)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    StarCeram® Z-Nature, StarCeram® Z-Smile

    FDA 510(k)
    FDA Class 2 ·Dental

    2243656-2001-00001

    FDA Adverse Event
    Injury ·Product code KGX·February 9, 2007

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 9, 2023

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ILS·November 11, 2014

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 24, 2011

    SENSOR BSA

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·July 23, 2013