BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    HOTLINE FLUID WARMER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    ZIRPRIME

    FDA 510(k)
    FDA Class 2 ·Dental

    MICRODOSE CATH, MODELS 90121-201, -202, -203

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    UNI LFIT MEDIAL FEMORAL COMP.

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code HRY·April 15, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·November 24, 2010

    OT VERIO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 3, 2014