BEUDAMED
    42 results · 35ms · Sources: EU EUDAMED, US FDA

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    CurvaFix Intramedullary Rodscrew System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORTHOMAP

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252355717·ORTHOMAP¿ EXPRESS KNEE 2.0 - SALES DEMO

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694004923·30 x 48mm Sub-Temporal Plate

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100500·Caddie, 4.75mm Screws

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009757·PedFuse ReTurn, SLD, 8.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009764·PedFuse ReTurn, SLD, 8.0mm x 55mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009795·PedFuse ReTurn, SLD, 8.0mm x 70mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009733·PedFuse ReTurn, SLD, 8.0mm x 40mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009788·PedFuse ReTurn, SLD, 8.0mm x 65mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009719·PedFuse ReTurn, SLD, 8.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009771·PedFuse ReTurn, SLD, 8.0mm x 60mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009818·PedFuse ReTurn, SLD, 8.0mm x 80mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009801·PedFuse ReTurn, SLD, 8.0mm x 75mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009726·PedFuse ReTurn, SLD, 8.0mm x 35mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009740·PedFuse ReTurn, SLD, 8.0mm x 45mm

    SPIRUS MEDICAL ENDO-EASE ENDOSCOPIC OVERTUBE

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

    R & D SYSTEMS XERET HEMATOLOGY CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    BD¿ LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·December 19, 2022

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·June 13, 2019

    Stimulator, Carotid Sinus Nerve

    FDA Pre-Market Approval
    FDA Class 3 ·BAROSTIM NEO® System