BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    MICRATOME MS7000 -ADVANCED CORNEAL/REFRACTIVE INSTRUMENTATION (ACRI)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981554·anteriors; shade A2 light; mould BIM6

    Stowe Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TOKUYAMA TISSUECARE

    FDA 510(k)
    FDA Class 2 ·Dental

    OPTI-FREE PLUS

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code LPN·December 12, 2017

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 27, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 31, 2011

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 5, 2014