BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    BeneVision Central Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Reveal

    FDA UDI
    Oticon A/S·05707131342393·G10, BTE 13 2.4G 85 C092 REVEAL

    SIMUPLAN TREATMENT PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    IVOBASE HYBRID, IVOBASE HIGH IMPACT

    FDA 510(k)
    FDA Class 2 ·Dental

    MIRU 1DAY UPSIDE (MIDAFILCON A)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 22, 2025

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·October 7, 2008

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    ANIMAS CORPORATION·Product code LZG·June 27, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·August 5, 2011

    FREESTYLE LIBRE 14 DAY

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC·Product code PZE·September 5, 2023

    FREE STYLE LIBRE 2

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC.·Product code QLG·June 10, 2022