BEUDAMED
    26 results · 23ms · Sources: EU EUDAMED, US FDA

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    Aquilion ONE Vision, v7.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1424650·14mm H x 24mm W x 65mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X14246580·14mm H x 24mm W x 65mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X142465120·14mm H x 24mm W x 65mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L142465120·14mm H x 24mm W x 65mm L XLIF Trial 12 degree L...

    BIPAP AVAPS VENTILATORY SUPPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PS MEDICAL STRATA II VALVE

    FDA 510(k)
    FDA Class 2 ·Neurology

    BIPAP A30

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 31, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 3, 2022

    BIPAP A30

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP A30

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 30, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 16, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Injury ·BAXTER HEATHCARE CORPORATION·Product code FKX·October 5, 2014