BEUDAMED
    11 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PROKERA

    FDA Adverse Event
    Injury ·Product code NQB·September 29, 2021

    PROKERA

    FDA Adverse Event
    Injury ·TISSUE TECH, INC.·Product code NQB·September 17, 2019

    BIOTISSUE

    FDA Adverse Event
    Injury ·Product code NQB·March 4, 2021

    PROKERA OPHTHALMIC BIOLOGICAL TISSUE

    FDA Adverse Event
    Malfunction ·TISSUETECH, INC.·Product code NQB·February 10, 2020

    PROKERA

    FDA Adverse Event
    Injury ·TISSUETECH INC·Product code NQB·August 2, 2019

    PROKERA

    FDA Adverse Event
    Injury ·Product code NQB·February 11, 2021

    PROKERA

    FDA Adverse Event
    Injury ·TISSUE TECH, INC.·Product code NQB·November 10, 2020

    PROKERA

    FDA Adverse Event
    Malfunction ·TISSUE TECH, INC.·Product code NQB·March 26, 2020

    PROKERA SLIM NON-STERILE BIOLOGICAL CORNEAL BANDAGE

    FDA Adverse Event
    Injury ·TISSUETECH, INC. / BIOTISSUE HOLDINGS, INC.·Product code NQB·May 16, 2025

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·December 10, 2021

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 7, 2023