BEUDAMED
    21 results · 43ms · Sources: EU EUDAMED, US FDA

    ISOMEDIX OPERATIONS INC.

    FDA registration
    ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

    PL Tubing Set (STERILE)

    FDA registration
    Engineered Medical Systems, LLC·1 product·🇺🇸 United States

    AccuLIF TL and PL Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ComfortDry

    FDA registration
    Ovik Health (a division of Miliken & Co)·1 product·🇺🇸 United States

    CREATEC GmbH & CO. KG

    FDA registration
    CREATEC GmbH & CO. KG·1 product·🇩🇪 Germany

    HAYWOOD VOCATIONAL OPPORTUNITIES

    FDA registration
    HAYWOOD VOCATIONAL OPPORTUNITIES·1 product·🇺🇸 United States

    ZimmerGmbH8803 (DK) - Zimmer Natural Nail™ System

    FDA registration
    Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

    ZNN Cephalomedullary Femoral Nail-Asia

    FDA registration
    ZIMMER GMBH·1 product·🇨🇭 Switzerland

    INTERDRY SILVER

    FDA registration
    C6 MEDICAL INCORPORATED (MEDNEEDLES & ADVWOUNDCARE)·1 product·🇨🇦 Canada

    Scorpio

    FDA UDI
    Howmedica Osteonics Corp.·07613154020591·Cruciate Retaining Tibial Insert

    B-P TOTAL HIP SYSTEM

    FDA UDI
    Synovo Production·00814193024589·B-P MODULAR EXTENSION W/ULTRACOAT - 15 MM X 175 MM

    Lacrimal Intubation Set

    FDA registration
    Oasis Medical, Inc.·1 product·🇺🇸 United States

    BLAZEJEWSKI MEDI-TECH GMBH

    FDA registration
    BLAZEJEWSKI MEDI-TECH GMBH·1 product·🇩🇪 Germany

    Elecsys CYFRA 21-1 CalSet

    FDA registration
    ROCHE DIAGNOSTICS GMBH·3 products·🇩🇪 Germany

    Isomedix Operations, Inc.

    FDA registration
    Isomedix Operations, Inc.·1 product·🇺🇸 United States

    ANODYNE SURGICAL

    FDA registration
    ANODYNE SURGICAL·1 product·🇺🇸 United States

    AUDIT MICROCV HOMOCYSTEINE LINEARITY SET, MODEL 704M-5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MODIFICATION TO: CARDIMA ABLATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    FDA classification
    FDA Class 2 ·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue