BEUDAMED
    137 results · 22ms · Sources: EU EUDAMED, US FDA

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    Coala Heart Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1820400·18mm H x 20mm W x 40mm L x 0 degrees XLIF

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528127520·2.0 X 40mm Cannulated Headed Screw, T7

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741820400·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X18204080·18mm H x 20mm W x 40mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L182040120·18mm H x 20mm W x 40mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X182040120·18mm H x 20mm W x 40mm L x 12 degrees XLIF

    KING Snap Lead/DIN Connector

    FDA UDI
    Kego Corporation·00663427000055·KING Snap Lead/DIN Connector Qty 5 1.0 m (40")...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674182040060·

    PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MINISILK FT

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

    PENTAX

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

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

    PENTAX

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

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·November 7, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 26, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021