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

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    HYDRADJUST IV UROLOGICAL TABLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    DUAL LUMEN CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Arrow Epidural Catheter Kit

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CUSA NXT CONSOLE - POOL

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES IRELAND LIMITED·Product code LFL·April 30, 2014

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 5, 2013

    ON-Q PAINBUSTER

    FDA Adverse Event
    Other ·I-FLOW CORPORATION·Product code MEB·December 8, 2010

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021