BEUDAMED
    2,566 results · 32ms · Sources: EU EUDAMED, US FDA

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    Flowart

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528103777·7.0 x 105mm Cannulated Screw, 32mm Thd

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528108130·7.0 x 105mm Cann Screw 32Thd Sterile 2Pk

    SAFI-GEL DAILY DISPOSABLE (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS, SAFI-GEL DAILY DISPOSABLE TORIC ( METHAFILCON

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DIACHECK BLOOD GLUCOSE MONITORING SYSTEM MODEL: PREMIUM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PULSE GEN MODEL 104

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·June 26, 2013

    HAIRMAX LASER BRUSH

    FDA Adverse Event
    Other ·LEXINGTON INTERNATIONAL, LLC·Product code OAP·August 2, 2011

    FILTERWIRE EZ EMBOLIC SYSTEM (3.5MM - 5.5MM)

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NFA·September 24, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·August 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·August 5, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·October 31, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·December 15, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·November 15, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·October 13, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 15, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·September 15, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·February 2, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·January 16, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 17, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·September 15, 2021