BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983129·posteriors; shade BL1; size XL; lower jaw

    SHARPS COMPLIANCE CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Medtronic Total Hip Arthroplasty System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 28, 2013

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 2, 2014

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·February 4, 2011