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

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    DSL 17A-OH PROGERSTERONE (DSL #6800)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MODEL 495-01 PACING LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    TRACH MATE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    WEBSTER QUADROPOLAR - FIXED

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·June 26, 2012

    EVIA DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code DXY·June 25, 2014

    MP20 INTELLIVUE PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 3, 2010

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·November 16, 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