BEUDAMED
    7 results · 38ms · Sources: EU EUDAMED, US FDA

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    G.U. CO. LTD.

    FDA registration
    G.U. CO. LTD.·1 product·🇯🇵 Japan

    G.A. YELLOWS CO., LTD

    FDA registration
    G.A. YELLOWS CO., LTD·2 products·🇯🇵 Japan

    CHEMOCLAVE® VENTED BAG SPIKE

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·December 31, 2024

    Bencox Mirabo PE Liner 36/44 Model Number: H1.L61.3644, UDI: 8806373852343

    FDA Recall
    Terminated ·CORENTEC CO., LTD Seobuk-gu 12 Yeongsanhong 1-gil Seobuk-gu, Cheonan-si Korea (the Republic of)·Product code LPH·February 27, 2017

    Portable X-ray system

    FDA Recall
    Open, Classified ·DIGIMED CO., LTD 401, 402, 406~411-ho, A-dong 101, Gasan digital 2-ro, Geumcheon-Gu Seoul Korea (the Republic of)·Product code EHD·June 19, 2025

    Meddevices Lifesciences B.V.

    Authorized representative
    🇳🇱 Netherlands·41 Manufacturers·2587 Devices

    Emergo Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·900 Manufacturers·22100 Devices