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

    In-Ka® Percutaneous Balloon Dilatation Catheter and Amplatz Sheath

    FDA registration
    Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

    In-Ka Percutaneous Balloon Dilatation Catheters, Amplatz Sheath

    FDA 510(k)
    FDA Unclassified ·Unknown

    Catheter, Nephrostomy

    FDA classification
    FDA Unclassified ·Catheter, Nephrostomy

    K201145

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

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780433859·Integra® Jarit® Kelly Retractor, 9-1/2", Hollow...

    24M - Nevada Energy - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588011639·24M - Nevada Energy - Metal

    ACCLARENT PIVOT Balloon Dilation Systems

    FDA registration
    Integra LifeSciences Corporation·3 products·🇺🇸 United States

    PRO-TOE

    FDA registration
    WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

    PRO-TOE

    FDA registration
    WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

    Next Generation Balloon Dilation System

    FDA registration
    Nitinol Devices & Components Costa Rica, S. R. L.·3 products·🇨🇷 Costa Rica

    Next Generation Balloon Dilation System

    FDA registration
    Mentor Texas LP·3 products·🇺🇸 United States

    Acclarent8881 (CR2) - ACCLARENT PIVOT™ Navigation Balloon Dilation System

    FDA registration
    Synergy Health AST, SRL·3 products·🇨🇷 Costa Rica

    ACCLARENT PIVOT Balloon Dilation Systems

    FDA registration
    ACCLARENT, INC.·3 products·🇺🇸 United States

    PleurX Peritoneal Catheter System

    FDA registration
    CAREFUSION 2200, INC.·1 product·🇺🇸 United States

    Sterigenics U.S., LLC

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

    PleurX Peritoneal Catheter System

    FDA registration
    CareFusion D.R. 203 Ltd.·1 product·🇩🇴 Dominican Republic

    POLYMER COATED POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NEW HEIGHTS ELECTRIC ELEVATING POWER WHEELCHAIR MODEL NO. 08 02 SERIES

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided

    FDA Pre-Market Approval
    FDA Class 3 ·EXABLATE

    Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided

    FDA Pre-Market Approval
    FDA Class 3 ·EXABLATE 2000 SYSTEM