BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    REVISED PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867241299·3.5mm Drill Sleeve, Short

    GIANTURCO-WALLACE TRACHEOBRONCHIAL Z STENT

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

    MODELS 432-03 & 433-03 IMPLANTABLE PACING LEADS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·January 16, 2014

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010

    CENTURY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·November 20, 2012

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·September 8, 2022