Guía y declaración del fabricante – Emisiones e inmunidad electromagnéticas

Guía y declaración del fabricante – emisiones electromagnéticas

El VPAP está diseñado para ser utilizado en el entorno electromagnético especificado a continuación. El cliente o usuario del VPAP deberá asegurarse de que sea utilizado en dicho entorno.

Prueba de emisiones

Cumplimiento

Entorno electromagnético –

guía

 

 

 

 

 

Emisiones de RF CISPR11

Grupo 1

El VPAP usa energía de RF sólo para

 

 

su funcionamiento interno. Por lo

 

 

tanto, sus emisiones de RF son muy

 

 

bajas y es improbable que provoquen

 

 

interferencias en equipos electrónicos

 

 

cercanos.

 

 

 

Emisiones de RF CISPR 11

Clase B

El VPAP es apropiado para ser usado

 

 

en todos los ámbitos, incluso ámbitos

 

 

Emisiones armónicas

Clase A

domésticos y aquéllos conectados

CEI 61000-3-2

 

directamente a la red pública de bajo

 

 

voltaje que abastece a los edificios

 

 

Fluctuaciones de voltaje/

Cumple

destinados a vivienda.

Emisiones de parpadeo

 

 

(“flicker”) CEI 61000-3-3

 

 

 

 

 

Un equipo médico eléctrico requiere precauciones especiales en lo concerniente a la compatibilidad electromagnética, y debe ser instalado y puesto en funcionamiento según la información relativa a dicha compatibilidad que se proporciona en este documento.

Advertencias: el sistema VPAP no debe utilizarse al lado de otro equipo, ni montarse sobre o debajo de otro equipo.

Si dicha proximidad o el tenerlo montado sobre otro equipo es necesario, el VPAP debe ser observado para verificar su normal funcionamiento en la configuración en la que será utilizado.

No se recomienda el uso de accesorios (por ej. humidificadores) distintos a los que se especifican en este manual. Dichos humidificadores podrían provocar un aumento de las emisiones o una disminución de la inmunidad del equipo VPAP.

Español

Especificaciones del sistema

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ResMed VPAPTm III$IIIst user manual Español

VPAPTm III$IIIst specifications

The ResMed VPAP™ III ST is a sophisticated bilevel positive airway pressure (BiPAP) device designed for patients with complex respiratory conditions such as obstructive sleep apnea and chronic obstructive pulmonary disease (COPD). It is renowned for its robust performance, user-friendly interface, and advanced features that enhance patient comfort and compliance.

One of the main features of the VPAP III ST is its easy-to-navigate display. The color LCD screen provides clear, concise information on treatment settings and patient usage data, which allows both healthcare providers and patients to monitor the effectiveness of the therapy. The device also offers a range of customizable settings, allowing it to cater specifically to individual patient needs.

Another remarkable aspect of the VPAP III ST is its Adaptive Servo-Ventilation (ASV) technology. This advanced algorithm continuously monitors the patient’s breathing patterns, adjusting the pressure in real-time to ensure optimal support during each respiratory cycle. This adaptability helps to maintain effective ventilation while minimizing discomfort that might arise from constant pressure settings.

The VPAP III ST features AutoSet™, a technology that automatically adjusts pressure levels based on detected airflow limitations. This feature enhances patient comfort by reducing pressure during exhalation and providing higher support during inhalation, creating a more natural breathing experience. This automatic adjustment means patients are less likely to experience the discomfort associated with forced ventilatory pressures.

Moreover, the device includes an integrated humidifier, which decreases the risk of upper airway irritation and dryness. The heated humidifier can be adjusted according to patient preferences and environmental conditions to provide optimal moisture levels during therapy.

In terms of portability, the VPAP III ST is designed to be user-friendly with innovative features such as a lightweight design, making it easier for patients to use at home or while traveling. The device is compatible with a variety of mask options, ensuring that patients can find a comfortable fit that suits their individual needs.

Additionally, the VPAP III ST offers comprehensive data reporting capabilities, allowing healthcare providers to track patient adherence and therapy effectiveness over time. This data can be invaluable in making adjustments to treatment plans and ensuring that patients remain on track with their therapy.

In conclusion, the ResMed VPAP™ III ST is a leading-edge respiratory therapy device that combines advanced technology with user-centric design. Its adaptive features, customizable settings, and built-in humidification contribute to an optimal treatment experience, ensuring patients receive the care they need for improved respiratory health.