BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    IONTOPHORESIS DEVICE - ELECTRODE RH 800

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PERRY* STERILE X-AM* GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    REAADS-RF TEST KIT-QUANTITATIVE

    FDA 510(k)
    FDA Class 2 ·Immunology

    TENDRIL ST

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

    SPECTRUM INFUSION PUMP

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

    TOTALCARE BARIATRIC

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

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020