BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    PNEUMOCYSTIS CARINII IMMUNOFLUORESCENCE TEST KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ARTIS icono

    FDA 510(k)
    FDA Class 2 ·Radiology

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODELS KD 5901, KD-7909,

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STEAM STER LOCKS ORANGE

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

    UNKNOWN ZIMMER KNEE

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

    MP50 INTELLIVUE PATIENT MONITOR

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

    NEXGEN LPS-FLEX FEMORAL COMPONENT

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

    STEAM STER LOCKS ORANGE

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