BEUDAMED
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    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    Prevena Plus 125 Therapy Unit

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    KCI NORTH IX (Technical Services Center)

    FDA registration
    KCI NORTH IX (Technical Services Center)·1 product·🇺🇸 United States

    InnoFine

    FDA UDI
    JingFang Precision Medical Device(Shenzhen) Co., Ltd.·06971554720505·Reusable Needle Guides for use with Philips PA4...

    HOOK,OESCH,SIZE I,HQ,S

    Device
    EU MDR · Eu Md Class 2a ·On the market

    Stent, Urethral, External Sphincter, Permanent

    FDA Pre-Market Approval
    FDA Class 3 ·UROLUME ENDOPROSTHESIS

    Vivace Ultra/Ultra Vision RF Microneedling Device

    FDA registration
    BOULDER BIOMED LLC·3 products·🇺🇸 United States

    Fibrinet

    FDA registration
    BOULDER BIOMED LLC·1 product·🇺🇸 United States

    Extremity All Suture System

    FDA registration
    BOULDER BIOMED LLC·3 products·🇺🇸 United States

    TenJet

    FDA registration
    BOULDER BIOMED LLC·1 product·🇺🇸 United States