Heartstart FRx Trainer

Heartstart FRx Trainer

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Heartstart FRx Trainer

Product Code 861306

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What's Included?

  • Heartstart FRx Trainer

 Simulando todas las funciones únicas del DEA  Heartstart FRx, la Unidad de Formación FRx le permitirá conocer a fondo su dispositivo clínico, proporcionando a los estudiantes una experiencia de entrenamiento práctica y realista.

Para encender su unidad de entrenamiento, simplemente inserte 4 pilas AA y podrá aprender cómo funciona su DEA, ya que le guiará paso a paso a través de todo el proceso de rescate.

Modo de Empleo

Proporcionar a los usuarios potenciales la formación previamente a un rescate real puede ser beneficioso para ayudar a los alumnos a entender el proceso de rescate completo, qué se puede esperar y cómo aplicar los electrodos rápida y eficazmente. Esto ayuda a crear confianza en la capacidad del usuario, fomentando un rescate más eficaz en caso de una emergencia.

Con ocho escenarios de rescate diferentes incorporados al dispositivo, los estudiantes pueden practicar la respuesta de diferentes maneras para obtener una comprensión completa de las características de la unidad, mientras que los electrodos de entrenamiento reutilizables ayudan a  aumentar el realismo de la experiencia.

Más información

¿Quieres saber más sobre el Heartstart FRx Trainer? Nuestro equipo defibshop está a sólo una llamada de distancia. Para ponerse en contacto, llame al 888 820 0760 donde uno de nuestros asesores le atenderá gustosamente.



 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.