BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    PARALLAX ACRYLIC RESIN WITH TRACERS TA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450051634·

    BD MAX¿ VAGINAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCH·December 3, 2025

    BD MAX¿ VAGINAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCH·December 3, 2025

    INTRASTENT DOUBLESTRUT XS STENT

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

    ANALYST PANELS + ANALYTICAL TEST ROTOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BD MAX¿ VAGINAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·November 17, 2025

    MICROBORE EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·November 29, 2016

    FREESTYLE FREEDOM

    FDA Adverse Event
    Malfunction ·Product code NBW·April 10, 2013

    RIATA ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    6461500 INFUSOR PUMP (1 LABEL)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·April 12, 2011

    BD MAX¿ VAGINAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·December 3, 2025

    BD MAX¿ VAGINAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·December 3, 2025

    BD PEGASUS¿ SAFETY CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·September 9, 2019