BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    MEPORE (6X7)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RECEIVING BLANKET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARx® SAI Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PORTEX 7.0MM VOCALAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC.·Product code CAZ·January 9, 2013

    ENDURON NEUT 54OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 5, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014