BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    OVERDENTURE ATTACHMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199212·AK3 Congruent Insert Trial Size 6, 13mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867221239·3.5mm Locking Post, Distractor

    TAKE 1

    FDA 510(k)
    FDA Class 2 ·Dental

    MODEL 72-81-0 UNVENTED SOLUTION ADM. SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ALFA HIP

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code LPH·June 24, 2014

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·October 18, 2010

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 7, 2012

    CONNECTOR, 1/4" X 1/4" STRAIGHT WITH LUER LOCK PORT

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code OEZ·April 26, 2016