BEUDAMED
    8 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SAFE PLACE PATIENT WANDERING

    FDA Adverse Event
    Injury ·RF TECHNOLOGIES, INC·Product code KMI·July 9, 2007

    TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAE·March 6, 2025

    QDOT MICRO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OAE·March 19, 2025

    VARIPULSE¿ BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code QZI·March 19, 2025

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DRF·August 4, 2025

    CODE ALERT

    FDA Adverse Event
    Injury ·R.F. TECHNOLOGIES, INC.·Product code KMI·June 6, 1997

    SENSATEC

    FDA Adverse Event
    Injury ·R.F. TECHNOLOGIES, INC.·Product code KMI·October 30, 2006

    SENSATEC

    FDA Adverse Event
    Injury ·R.F. TECHNOLOGIES, INC.·Product code KMI·December 29, 2004