Manual para Evia HF(-T)

Manual para Evia HF(-T)

Marca: BIOTRONIK

Categoría: Medical Devices

Tipo de Documento: Manual

Idioma: ES

Idiomas Disponibles: EN , ES

Subido: 20 de abril de 2026 a las 20:00

Fecha de Publicación del Manual: 2013-09-06

Información de Garantía

Warranty information is not explicitly stated in the provided manual sections.

Device Operation Summary

The Evia HF(-T) is an implantable pacemaker system designed for bradycardia arrhythmia indications. Its primary objective is to improve patient symptoms through pacing and cardiac resynchronization therapy. Key functions include automatic rhythm monitoring, bradycardia treatment, biventricular pacing for resynchronization, and comprehensive diagnostic capabilities. The system integrates with BIOTRONIK Home Monitoring® for remote therapy management. The device family includes triple-chamber models like Evia HF and Evia HF-T, utilizing NBG code DDDRV. It supports various pacing modes and offers features like auto-initialization, capture control, and rate adaptation. The programmer facilitates device interrogation, data storage, and function monitoring.

Solución de problemas y códigos de error

Issue/Symptom Possible Cause Solution/Action
Inadequate therapy due to defective device Dropped device during handling Use a replacement device. Send damaged device to BIOTRONIK.
Short circuit due to open lead connector ports Open connector ports in the header Close unused connections with blind plugs.
Inadequate therapy (leads not spaced sufficiently) Leads not spaced apart or positioned inappropriately Ensure leads are sufficiently spaced; ensure tip and ring electrodes do not touch.
Possible far-field sensing or insufficient defibrillation Lead dislocation or improper positioning Ensure proper lead placement and spacing.
Potential interference with device function Electromagnetic interference (EMI) sources Minimize exposure to EMI sources; follow guidelines for specific procedures (e.g., MRI, radiation therapy).
Política de Privacidad