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

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    VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150751·K-WIRE - SINGLE TROCAR 1.25mm DIA x 200mm

    AxSOS 3 Ti Locking Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROVOX NID VOICE REHABILITATION SYSTEM, MODEL REF 7101 TO 7134

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

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 13, 2012

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 30, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2014