ZOLL AED Pro SurePower Rechargeable Lithium Ion Battery Pack

ZOLL AED Pro SurePower Rechargeable Lithium Ion Battery Pack

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ZOLL AED Pro SurePower Rechargeable Lithium Ion Battery Pack

Product Code 8019-0535-01USA

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What's Included?

  • Batería recargable AED Pro

Esta batería recargable AED Pro de Zoll es una solución rentable para mantener su DEA completamente cargado en todo momento.

Normalmente, las baterías de los DEA deben ser reemplazadas después de aproximadamente 5 años; sin embargo eligiendo una opción recargable, usted puede tener la confianza de que su DEA tiene siempre la energía para realizar los cuidados de salvamento una víctima de paro cardiaco.

Características

  • Batería recargable
  • Avisos de voz y texto "Change Battery"
  • Autocomprobaciones automáticas del cargador de baterías y desfibrilador

 

Modo de Empleo

Primero, compruebe que la batería esté completamente cargada antes de la instalación. Inserte la batería en el dispositivo y su DEA comenzará automáticamente el proceso de auto-verificación.

Se le avisará de cualquier aspecto defectuoso de su dispositivo que pueda requerir su atención, como electrodos desconectados o batería baja.

Para iniciar el procedimiento de desfibrilación, todo lo que necesitará hacer es conectar los electrodos, encender el dispositivo y esperar más instrucciones.

No recomendamos usar una batería parcialmente cargada en un desfibrilador, ya que no podrá alcanzar su máximo potencial. El símbolo de "batería lista" se iluminará en el cargador una vez que esté listo para su uso.

Más Información

¿Está considerando la compra de la Batería Recargable AED Pro? Nuestros asesores defibshop están a mano para atender su llamada si tiene alguna pregunta antes de comprar. Llame al 888 820 0760 para hablar con nuestro equipo directamente.

 Want to know why you should choose us? 

  • Experienced and knowledgeable staff on-hand to offer impartial advice on all things AEDs
  • We have a nationwide training network to deliver training in the use of a defib and CPR
  • Not only providing free battery and pad reminders, we also will replace your electrode pads for free if you use your defib in the first two years after purchase
  • Over 14 years worth of experience as an AED specialist 
  • 5 / 5 Review Score
  • Over 97% of our customers would buy from us again

 

What is an IP rating?

An IP (Ingress Protection) rating classifies the degrees of protection of an electrical item against water and dust. Beginning with IP and followed by two numbers, the first digit is indicative of the item’s resistance to dust and the second is of its resistance to water. Protection against dust is measured from */ 0 up to 6, whereas protection against water is measured from */ 0 up to 8. The protection against these elements increases as the number does, with * / 0 telling us that the item has NO protection against either dust or water.

Why is this important?

The IP rating of a defib will tell you (and us!) whether it is suitable for the environment where it’s most likely to be used; for example, if there is a good chance your defib may be used in an outdoor environment, you will need a unit with a higher IP rating to ensure it can be used regardless the weather or terrain. If you are looking for a defibrillator more suitable for an indoors environment, you can afford to choose one with a lower IP rating, based on the other features that may be more suitable.

When a particular product is “approved” by the FDA, this marks the pass in the premarket approval (or PMA) application of a particular product which has been submitted to the FDA.

To receive approval of a device through a PMA application, the applicant in question must provide reasonable assurance of the device’s safety and effectiveness which is then challenged by the FDA before being approved.

Whilst all AEDs can be used to increase chances of survival and even save a life in the event of a cardiac arrest, FDA approved devices provide that extra piece of mind that the specific unit being used has undergone vigorous and substantial testing to ensure that that particular piece of equipment operates just as it should and provides the most effective care possible.

Many manufacturers perform their own tests on products, but not all defibrillators will undergo the same premarket approval as FDA approved devices and there is no guarantee or stamp of certification if testing has taken place with non-FDA approved products.