BEUDAMED
    18 results · 42ms · Sources: EU EUDAMED, US FDA

    JET™7Reperfusion Catheter with MAX Delivery Device (JET™7MAX)

    FDA registration
    PENUMBRA, INC.·1 product·🇺🇸 United States

    Penumbra System (Reperfusion Catheters, Separators, Aspiration Tubing, and 3D Revascularization Device)

    FDA registration
    Sterigenics U.S., LLC·1 product·🇺🇸 United States

    JET™7Reperfusion Catheter with MAX Delivery Device (JET™7MAX)

    FDA registration
    Penumbra Inc.·1 product·🇺🇸 United States

    JET™7Reperfusion Catheter with MAX Delivery Device (JET™7MAX)

    FDA registration
    Penumbra Inc.·1 product·🇺🇸 United States

    JET™7Reperfusion Catheter with MAX Delivery Device (JET™7MAX)

    FDA registration
    Penumbra Inc.·1 product·🇺🇸 United States

    Penumbra System Penumbra JET 7X

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Catheter, Thrombus Retriever

    FDA classification
    FDA Class 2 ·Catheter, Thrombus Retriever

    K191943 SYMPHONY Navigation Ready Instruments, Universal Navigation Adaptor Set (UNAS)

    FDA registration
    EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

    Oticon

    FDA UDI
    Oticon A/S·05707131339973·SIYA 2, KIT 312 2.4G NFM R C001

    Axis-Shield Active-B12 (Holotranscobalmin)

    FDA registration
    AXIS-SHIELD DIAGNOSTICS, LTD.·1 product·🇬🇧 United Kingdom

    VIDAS TOXO IgG Avidity

    FDA registration
    BIOMERIEUX SA·1 product·🇫🇷 France

    Prosthesis, Chin

    FDA registration
    Stryker Sustainability Solutions Phoenix·1 product·🇺🇸 United States

    TDS Standard Solution

    FDA registration
    MESA LABORATORIES, INC.·1 product·🇺🇸 United States

    Synergy Health AST, SRL

    FDA registration
    Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica

    VIDAS TOXO IGG AVIDITY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VLIFT-S VERTEBRAL BODY REPLACEMENT SYSTEM, MODELS 488812XX, 488814XX, 488816XX, 488818XX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

    FDA classification
    FDA Class 2 ·Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

    Spinal Vertebral Body Replacement Device

    FDA classification
    FDA Class 2 ·Spinal Vertebral Body Replacement Device