BEUDAMED
    189 results · 46ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    BELOS VR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH & CO.·Product code MKJ·July 24, 2003

    BELOS VR

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH & CO.·Product code MKJ·July 24, 2003

    GUARDIAN SYSTEM

    FDA Adverse Event
    Malfunction ·AVERTIX MEDICAL INC.·Product code QBI·June 2, 2025

    DEXTRUS 4135

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVZ·May 11, 2012

    SETROX S 60

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVZ·June 22, 2012

    DEXTRUS 4136

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code DTB·May 21, 2012

    DEXTRUS 4136

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVZ·June 22, 2012

    DEXTRUS 4136

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVZ·February 8, 2012

    LUMAX

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code MRM·October 17, 2017

    RIGHT VENTRICULAR LEAD

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVN·July 26, 2024

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code LWS·August 23, 2024

    PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVY·July 2, 2024

    LINOX SD 65/18

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code LWS·November 4, 2010

    RV LEAD

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVY·June 5, 2024

    LUMAX 540

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code LWS·February 20, 2013

    PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVY·October 23, 2025

    DEXTRUS 4135

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVZ·February 26, 2013

    RX45JBP

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code DTB·May 28, 1999

    LV LEAD

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code OJX·October 14, 2025

    LINOX SMART SD 65/18 HIGH VOLTAGE TACHY LEAD

    FDA Adverse Event
    Malfunction ·BIOTRONIK, INC.·Product code NVY·February 28, 2014