BEUDAMED
    90 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    Endotronix Inc.

    Manufacturer
    🇺🇸 United States

    Cordella Sensor Delivery Kit

    FDA UDI
    Endotronix, Inc.·00850008997006·The Cordella Pulmonary Artery Sensor System is ...

    Cordella Calibration Equipment

    FDA UDI
    Endotronix, Inc.·00850008997020·The Cordella Pulmonary Artery Sensor System is ...

    myCordella Handheld Patient Reader

    FDA UDI
    Endotronix, Inc.·00850008997013·The Cordella Pulmonary Artery Sensor System is ...

    myCordella Handheld Patient Reader Alloy

    FDA UDI
    Endotronix, Inc.·00850008997143·The Cordella Pulmonary Artery Sensor System is ...

    Cordella Data Analysis Platform

    FDA UDI
    Endotronix, Inc.·00850008997051·The Cordella Pulmonary Artery Sensor System is ...

    myCordella Patient Management Portal

    FDA UDI
    Endotronix, Inc.·00850008997044·myCordella Patient Management Portal is a compo...

    myCordella Patient Kit

    FDA UDI
    Endotronix, Inc.·00850008997068·myCordella Patient Kit consists of the myCordel...

    myCordella Patient App

    FDA UDI
    Endotronix, Inc.·00850008997037·myCordella Patient App is a component of the my...

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·August 28, 2024

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·September 10, 2024

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Malfunction ·ENDOTRONIX, INC·Product code MOM·August 28, 2024

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·August 20, 2024

    CORDELLA PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·July 29, 2024

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·September 23, 2024

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·September 10, 2024

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Malfunction ·ENDOTRONIX, INC·Product code MOM·September 10, 2024

    CORDELLA PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·May 22, 2026

    CORDELIA PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·April 22, 2026

    CORDELLA¿ PULMONARY ARTERY SENSOR SYSTEM

    FDA Adverse Event
    Injury ·ENDOTRONIX, INC·Product code MOM·December 16, 2025