BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    VIROTHERM HUMIDIFIER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PHILIPS GYROVIEW-HR IMAGING WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOOP RETRIEVER

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

    TITAN TOUCH

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·May 12, 2022

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·June 11, 2014

    SROM*STM ST,30+4L NK,18X13X160

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code JDI·January 15, 2013

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·December 4, 2007