BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    LABEL, STERILIZATION INDICATOR; RADIATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Injury ·AESCULAP INC·Product code KCT·October 12, 2016

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code KCT·July 26, 2016

    NOVATION CFS PRESS-FIT AND CEMENTED STEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SurgicalAR

    FDA 510(k)
    FDA Class 2 ·Radiology

    NEXGEN LPS-FLEX OPTION FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NJL·June 4, 2014

    MP30 INTELLIVUE PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 1, 2010

    UNKNOWN ZIMMER SEGMENTAL KNEE

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code JWH·December 21, 2012