BEUDAMED
    2,937 results · 32ms · Sources: EU EUDAMED, US FDA

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    RadialSeal Introducer Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741818550·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674181855060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1818550·18mm H x 18mm W x 55mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L181855120·18mm H x 18mm W x 55mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X18185580·18mm H x 18mm W x 55mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X181855120·18mm H x 18mm W x 55mm L x 12 degrees XLIF

    IMPAIR AWARE ALCOHOL LEVEL INDICATION SYSTEM (ALIS)

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    PROFAST+ ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    UNKNOWN SUTURE PRODUCT

    FDA Adverse Event
    Injury ·ETHICON, INC SOMERVILLE·Product code GAK·July 28, 2011

    ECHELON*FLEX45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 21, 2013

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 14, 2022

    311NNM NARROWAND UV PHTOTHERAPY LIGHT LAMP

    FDA Adverse Event
    Injury ·XUZHOU KERNEL MEDICAL INSTRUMENT EQUIPMENT CO LTD.·Product code FTC·December 22, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 6, 2021

    PENTAX

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

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·September 28, 2021