BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    PRESSURE INFUSION CUFF

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Biomet Tibial trays

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    BMT GB KNEE STM 12X40

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OIY·June 1, 2022

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013

    VERTEX EPIC - GAMMA CAMERA SYSTEMS

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code KPS·November 16, 2010

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MPRI·Product code NVY·July 17, 2014

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code HQL·April 1, 2022

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING NETHERLANDS·Product code HQL·April 1, 2022