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

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    SENTRY ANTERIOR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARIES INDICATOR

    FDA 510(k)
    FDA Class 2 ·Dental

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013

    CONSERVE(R) PLUS SPIKED CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·December 16, 2010

    MINILINK TRANSMITTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 12, 2014