BEUDAMED
    209 results · 31ms · Sources: EU EUDAMED, US FDA

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    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·HYMOVIS

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·HYMOVIS

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·HYMOVIS®

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·HYMOVIS® (High Molecular Weight Viscoelastic Hyaluronan)

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·HYMOVIS ONE

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·HYMOVIS®

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169502543·PLATE 2150010 OLIF51 PLATE 10MM

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·14026704629623·Rusch Polaris FO Blade, Miller 1

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·14026704711748·Rusch Polaris FO Blade, Miller 1

    CASE MEDICAL

    FDA UDI
    Case Medical Inc.·00653159010125·IR CAMERA TRAY

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022408·KLEOS PSL METAL ROTH 022 LL4 PK5

    batrik Arc Wire Brushes Reusable

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521008496·Brush/Red/BD 10mm/BL 50mm/OL 45cm - Rigid - REU...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707069201·LIGATURE THREADER

    Sorrento Bone Graft Substitute Strip (12cc)

    FDA UDI
    XENCO MEDICAL LLC·B064HB11500101·Sorrento Bone Graft Substitute Strip (12cc) 10c...

    Batrik Brush/Red/BD 10mm/BL 50mm-SN

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521008502·Brush/Red/BD 10mm/BL 50mm/OL 45cm - Rigid - SIN...

    Cedic Oral/Luer Enteral ENFit Transition Connector for Medication Port

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NA

    FDA UDI
    Zimmer, Inc.·00889024033610·

    CONTOUR PLUS LINK 2.4

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·May 19, 2020

    CXDI CCS NE VER.1.40.2

    FDA Adverse Event
    Malfunction ·CANON, INC·Product code MQB·May 17, 2013

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code LOX·July 5, 2011