BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    OrthoGold

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Oticon

    FDA UDI
    Oticon A/S·05707131340122·SIYA 2, KIT 312 NFM L C001

    MODIFIED CONCENTRIC MICROCATHETER, MODEL 90047

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TIGERPAW SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·March 8, 2026

    BD KIESTRA IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·January 13, 2014

    DIGOXIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code KXT·August 4, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    BD Q-SYTE¿ LUER ACCESS SPLIT SEPTUM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 18, 2018