Cardiac Science Powerheart G3 AED backpack with quick-access front pouch

Cardiac Science Powerheart G3 AED backpack with quick-access front pouch

Imagenes Adicionales

Cardiac Science Powerheart G3 AED backpack with quick-access front pouch

Product Code 168-0064-001USA

0 reviews

En existencia

What's Included?

  • Mochila AED Rescue

Adecuado para el uso con la gama Cardiac Science Powerheart G3 AED, esta solución de almacenamiento y transporte le permitirá llevar su DEA en cualquier momento.

La Mochila AED Rescue tiene la capacidad de no sólo ser transportable, sino que además tiene espacio para transportar los accesorios vitales que serían esenciales si alguien fuese víctima de un paro cardiaco. Tener el DEA y los accesorios le permite crear un entorno “cardioprotegido”, sin importar dónde vaya, protegiéndose a sí mismo y a otros.

Modo de Empelo

La funda está diseñada para proteger su DEA de la exposición a los elementos incluyendo polvo, arena y agua para que pueda tener la confianza de que su DEA está siempre en condición óptima para rescate.

Con espacio suficiente para los accesorios, puede guardar un kit de rescate, electrodos adultos y pediátricos de repuesto y baterías, lo que le da la capacidad y confianza para reaccionar y responder en cualquier situación de emergencia.

El diseño de la mochila ayudará a los rescatadores a transportar con seguridad el DEA y los accesorios a cualquier lugar que deseen, ya sea un centro deportivo o una ubicación remota difícil de alcanzar.

Acerca del Fabricante

Cardiac Science es uno de los fabricantes de DEA más prestigiosos del mundo, proporcionando a los servicios de emergencia y al público en general dispositivos fáciles de usar y que salvan vidas.

El tiempo es un factor vital en el tratamiento a una víctima de un paro cardiaco y los dispositivos Powerheart hacen del aparentemente difícil proceso de salvar una vida, fácil, eliminando los retrasos innecesarios.

Más Información

Si desea más información sobre la Mochila AED Rescue, el equipo defibshop estará a su disposición para ayudarle.

Con más de una década de conocimiento y experiencia al otro lado del océano, uno de nuestros expertos asesores estará encantado de ayudar con sus consultas. Contáctenos hoy llamando al 888 820 0760.

 

 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.