BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    PORGES BIOPSY & FOREIGN BODY FORCEPS

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

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MICROLITE TUBE LUMINOMETER #011-902-0000

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CLARION IMPLANT

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·May 16, 2014

    TENDRIL ST

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

    APEX ARC HIP STEM

    FDA Adverse Event
    Injury ·OMNLIFE SCIENCE, INC.·Product code LZO·December 28, 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