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

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    GentleCath Glide Intermittent Catheter

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517566942·CoRoent Ant TLIF PEEK, 16x11x34mm 4°

    Ceramco® II Silver™

    FDA UDI
    Dentsply International Inc.·D0011613440·

    EXCIA TOTAL HIP SYSTEM LATERAL OFFSET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    G+ SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LOGIC CR TIB INSERT SLOPE+, SZ 5, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 9, 2023

    COMPR WIRE Ø1.6 L150/30

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWN·June 11, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Death ·CORDIS DE MEXICO·Product code NIQ·September 12, 2008