BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    OXFORD VDT-40 DISPLAY TERMINAL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209107780·

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981163228·Threaded Plate Locking Cover, 7mm

    ACCUREX GLUCOSE TEST STRIP

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Extended Range Shifter for PROBEAT-V

    FDA 510(k)
    FDA Class 2 ·Radiology

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 6, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 3, 2023

    DISTAL RESECTION GUIDE STAND

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·June 5, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·October 4, 2010

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code GCX·November 12, 2012