BEUDAMED
    18 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SURPASS EVOLVE 4.5MM X 20MM - PMAS

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 11, 2024

    SURPASS EVOLVE 3.25MM X 17MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 4, 2024

    SURPASS EVOLVE 4.0MM X 12MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 5, 2024

    SURPASS EVOLVE 4.0MM X 17MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 9, 2024

    SURPASS EVOLVE 4.0MM X 17MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 9, 2024

    SURPASS EVOLVE 3.25MM X 12MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 6, 2024

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·January 20, 2020

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·June 4, 2019

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·June 28, 2019

    SURPASS EVOLVE 4.5MM X 15MM - CE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·January 20, 2020

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·November 26, 2019

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·October 16, 2019

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    BRAUN

    FDA Adverse Event
    Injury ·KAZ, INC.·Product code FLL·July 12, 2011

    INS8400 WITH ONE FOOT OF PROXIMAL PATIENT LINE

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·September 8, 2017