BEUDAMED
    19 results · 36ms · Sources: EU EUDAMED, US FDA

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    ClariFix

    FDA UDI
    ARRINEX, INC.·00868438000203·Cryotherapy Device

    ClariFix

    FDA UDI
    ARRINEX, INC.·00868438000227·Cryogen Canister, 10ml

    ClariFix

    FDA UDI
    ARRINEX, INC.·00868438000258·Cryogen Canister

    ClariFix

    FDA UDI
    ARRINEX, INC.·00868438000210·Cryogen Canister, 21ml

    ClariFix

    FDA UDI
    ARRINEX, INC.·00868438000234·Cryotherapy System

    CLARIFIX II SYSTEM, US

    FDA Adverse Event
    Injury ·ARRINEX, INC.·Product code GEH·April 26, 2021

    CLARIFIX II SYSTEM, US

    FDA Adverse Event
    Injury ·ARRINEX, INC.·Product code GEH·April 26, 2021

    CLARIFIX II SYSTEM, US

    FDA Adverse Event
    Injury ·ARRINEX, INC.·Product code GEH·December 21, 2020

    CLARIFIX

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·October 18, 2018

    CLARIFIX

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·September 10, 2018

    CLARIFIX DEVICE

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·August 24, 2017

    CLARIFIX DEVICE

    FDA Adverse Event
    Injury ·ARRINEX, INC.·Product code GEH·May 10, 2017

    UNKNOWN_ARRINEX_PRODUCT

    FDA Adverse Event
    Injury ·ARRINEX, INC.·Product code GEH·March 23, 2020

    UNKNOWN_ARRINEX_PRODUCT

    FDA Adverse Event
    Injury ·ARRINEX, INC.·Product code GEH·March 3, 2020

    CLARIFIX

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·April 8, 2018

    CLARIFIX

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·September 13, 2019

    CLARIFIX

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·October 25, 2019

    CLARIFIX

    FDA Adverse Event
    Injury ·ARRINEX, INC·Product code GEH·November 25, 2019

    CLARIFIX

    FDA Adverse Event
    Malfunction ·ARRINEX, INC.·Product code GEH·November 27, 2019