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

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    ENDOPOUCH PRO SPECIMEN RETRIEVAL BAG

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981579·anteriors; shade A3 light; mould BIM2

    INVENTUS IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    eLens Rigid Gas Permeable Contact Lens for Daily Wear, eLens Rigid Gas Permeable Contact Lens for Daily Wear Ortho-K

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    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

    7700

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

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·August 5, 2014