BEUDAMED
    37 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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
    Malfunction ·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
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

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

    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 15MM - IDE

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

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·August 14, 2008

    FLEXCATH STEERABLE SHEATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·June 10, 2011

    UNKNOWN_NEUROVASCULAR_PRODUCT

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

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code OUT·December 16, 2019

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code OUT·December 23, 2019