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

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    Endoform Dental Membrane

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517630476·CoRoent Ant TLIF Ti, 13x11x30mm 15°

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776299187·KNOT PUSHER, CLOSED END, W LOOP

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 24, 2003

    OLYMPUS ULTRASONIC SURGICAL SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    CHISON DIAGNOSTIC ULTRASOUND SYSTEM, CONVEX PROBE, LINCAR PROBE, PHASED PROBE

    FDA 510(k)
    FDA Class 2 ·Radiology

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·November 17, 2008

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·July 25, 2011

    ECLIPSE

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR·Product code DTK·July 11, 2013

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025