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

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    NEURAVI LIMITED

    FDA registration
    NEURAVI LIMITED·2 products·🇮🇪 Ireland

    EMBOGUARD

    FDA UDI
    NEURAVI LIMITED·10886704082743·EMBOGUARD Balloon Guide Catheter

    EMBOTRAP

    FDA UDI
    NEURAVI LIMITED·10886704082866·EMBOTRAP III 5 x 22 mm Revascularisation Device

    EMBOGUARD

    FDA UDI
    NEURAVI LIMITED·10886704082736·EMBOGUARD Balloon Guide Catheter

    Embotrap

    FDA UDI
    NEURAVI LIMITED·10886704081326·EMBOTRAP II 5X33 REVASCULARISATION. DEVICE

    EMBOTRAP

    FDA UDI
    NEURAVI LIMITED·10886704084570·EMBOTRAP III 5 x 37 mm Revascularisation Device

    EMBOTRAP

    FDA UDI
    NEURAVI LIMITED·10886704082859·EMBOTRAP III 6.5 x 45 mm Revascularization Device

    Embotrap

    FDA UDI
    NEURAVI LIMITED·10886704081319·EMBOTRAP II 5X21 REVASCULARISATION DEVICE

    EMBOTRAP II 5X21 REVASC. DEV.

    FDA Adverse Event
    Malfunction ·NEURAVI LIMITED·Product code NRY·October 5, 2018

    EMBOTRAP II 5X33 REVASC. DEV.

    FDA Adverse Event
    Malfunction ·NEURAVI LIMITED·Product code NRY·November 15, 2018

    EMBOTRAP II 5X33 REVASC. DEV.

    FDA Adverse Event
    Malfunction ·NEURAVI LIMITED·Product code NRY·November 15, 2018

    EMBOTRAP II 5X33 REVASC. DEV.

    FDA Adverse Event
    Malfunction ·NEURAVI LIMITED·Product code NRY·February 20, 2019

    EMBOTRAP II 5X33 REVASC. DEV.

    FDA Adverse Event
    Malfunction ·NEURAVI LIMITED·Product code NRY·September 18, 2018

    EMBOTRAP II 5X33 REVASC. DEV.

    FDA Adverse Event
    Injury ·NEURAVI LIMITED·Product code NRY·August 23, 2018

    CERENOVUS EMBOGUARD

    FDA Adverse Event
    Malfunction ·CERENOVUS, INC. / NEURAVI LIMITED·Product code QJP·December 22, 2022

    RESTYLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·July 19, 2017

    RESTYLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·July 19, 2017

    RESTYLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·July 19, 2017

    RESTYLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·July 19, 2017

    RESTYLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·July 19, 2017