BEUDAMED
    18 results · 55ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    RIGHT ATRIAL (RA) LEAD

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code NVN·September 27, 2024

    RIGHT VENTRICULAR (RV) LEAD

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code NVN·September 27, 2024

    CELERITY

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code LWS·April 15, 2024

    SONTRTIP

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code LWS·April 15, 2024

    IMPLANTABLE PACEMAKER PULSE-GENERATOR

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code DXY·May 15, 2024

    RIGHT ATRIAL LEAD

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code NVN·February 13, 2024

    RIGHT VENTRICULAR LEAD

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code NVN·February 13, 2024

    IMPLANTABLE PACEMAKER PULSE-GENERATOR

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code DXY·December 5, 2024

    SORIN OVATIO ICD VR-IMPLANTED

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code MRM·March 17, 2020

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR RIGHT ATRIAL (RA)

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code LWS·January 31, 2025

    ELAPASSP752

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code NVN·January 13, 2026

    9758/58

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code NVN·January 13, 2026

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR RIGHT VENTRICULAR (RV)

    FDA Adverse Event
    Injury ·SORIN CRM SAS·Product code LWS·January 31, 2025

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MICROPORT / SORIN CRM SAS·Product code NVZ·October 8, 2025

    DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

    FDA Adverse Event
    Injury ·ELA / SORIN CRM SAS·Product code NVN·December 12, 2025

    DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER

    FDA Adverse Event
    Injury ·SORIN BIOMEDICAL/ SORIN CRM SAS·Product code MRM·May 2, 2025

    DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER

    FDA Adverse Event
    Injury ·SORIN BIOMEDICAL, INC./SORIN CRM SAS·Product code MRM·September 15, 2023

    VEGA STEROID-ELUTING ENDOCARDIAL LEADS (VEGA R52)

    FDA Adverse Event
    Injury ·MICROPORT CRM USA INC./ SORIN CRM SAS·Product code NVN·July 14, 2025