BEUDAMED
    11 results · 42ms · 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.
    Filters FDA Adverse Event ×

    COAG-SENSE

    FDA Adverse Event
    Injury ·COAGUSENSE, INC.·Product code GJS·August 31, 2023

    COAG-SENSE

    FDA Adverse Event
    Malfunction ·COAGUSENSE INC.·Product code GJS·April 6, 2020

    COAGSENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE INC.·Product code GJS·June 21, 2023

    TEST, TIME, PROTHROMBIN

    FDA Adverse Event
    Malfunction ·COAGUSENSE, INC·Product code GJS·March 23, 2020

    COAG-SENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE, INC·Product code GJS·February 17, 2026

    COAG-SENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE, INC.·Product code GJS·March 18, 2026

    COAG-SENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE INC·Product code GJS·January 13, 2026

    COAG-SENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE, INC.·Product code GJS·March 9, 2026

    COAG-SENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE, INC.·Product code GJS·March 18, 2026

    COAG-SENSE PT/INR MONITORING METER

    FDA Adverse Event
    Injury ·COAGUSENSE, INC·Product code GJS·January 29, 2026

    COAG-SENSE PT/INR SYSTEM

    FDA Adverse Event
    Malfunction ·COAGUSENSE INC·Product code GJS·March 8, 2022