BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    EPM-3300 VIDEO PROCESSOR

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

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·May 23, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·February 4, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·September 14, 2021

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867060067·ARTHREX ECLIPSE HUMERAL HEAD, 49/18

    LASERSCOPE'S MICROSPOT DERMASTAT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BELSCOPE LARYNGOSCOPE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    FRESENIUS 2008K

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 23, 2014

    PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·January 25, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·December 21, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 20, 2023