BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    GASTRIC LAVAGE KIT-DISPOSABLE

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

    Midwest® Phoenix™

    FDA UDI
    SIRONA Dental Systems GmbH·E2767914000·Midwest® Phoenix™ PM

    MODIFICATION TO AVIE A1C TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    Voyager Trajectory Array Guide (V-TAG)

    FDA 510(k)
    FDA Class 2 ·Neurology

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 22, 2015

    CUSTOM PAK

    FDA Adverse Event
    Malfunction ·ALCON - BELGIUM/ S.A. ALCON-COUVREUR N.V.·Product code KYG·August 6, 2010