BEUDAMED
    7 results · 16ms · Sources: EU EUDAMED, US FDA

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    CARDIOMEGA-T

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE LATEX PATIENT EXAMINATION GLOVES, TESTED FOR USE WITH CHEMOTHERAPY DRUGS WITH A PROTEIN CONTENT LABEL CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AMSCO 600 Steam Sterilizer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VIPERWIRE

    FDA Adverse Event
    Malfunction ·CARDIOVASCULAR SYSTEMS INCORPORATED·Product code DQX·October 4, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 7, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 13, 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