BEUDAMED
    63 results · 21ms · Sources: EU EUDAMED, US FDA

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    Agent, Absorbable Hemostatic, Non-Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·PerClot® Polysaccharide Hemostatic System

    Agent, Absorbable Hemostatic, Non-Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·PerClot® Polysaccharide Hemostatic System

    Agent, Absorbable Hemostatic, Non-Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·PerClot® Polysaccharide Hemostatic System

    Agent, Absorbable Hemostatic, Non-Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·PerClot Polysaccharide Hemostatic System

    Agent, Absorbable Hemostatic, Non-Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·PerClot® Polysaccharide Hemostatic System

    Agent, Absorbable Hemostatic, Non-Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·PerClot Polysaccharide Hemostatic System

    Trulife

    FDA UDI
    Trulife Limited·00645517531441·BARBARA PINK LACE ACCENT MASTECTOMY BRA P210A36

    Trulife

    FDA UDI
    Trulife Limited·00645517531557·BARBARA PINK LACE ACCENT MASTECTOMY BRA P210B36

    AMPLITUDE

    FDA UDI
    AMPLITUDE SAS·03701089500838·Resurfacing Patellar Implant NM Cemented Ø 36 mm

    Direct Plastic Cylinder Round

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011093·

    Direct Plastic Cylinder Round

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141587·Direct Plastic Cylinder Round

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319744147·Dingman Periosteal Elevator 8-1/4" (21cm), slig...

    Salvo® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642174380·8.5 x 55 mm Bone Screw, Cannulated, 3 mm Pitch

    Admiral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981278168·Cervical Plate, 2 Level, 36mm

    EXPLOR

    FDA UDI
    Biomet Orthopedics, LLC·00880304210424·

    Carnation Ambulatory Monitor (CAM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Stimulator, Tibial, Electrical, Implantable, For Urinary Incontinence

    FDA Pre-Market Approval
    FDA Class 3 ·eCoin Peripheral Neurostimulator

    Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Thoraflex™ Hybrid

    SYRINGE 50ML LL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 8, 2021

    Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Thoraflex Hybrid