Philips FR2 Pediatric Training Pads

Philips FR2 Pediatric Training Pads

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Philips FR2 Pediatric Training Pads

Product Code M3871AUSA

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Ayudándole a proporcionar la experiencia de entrenamiento más efectiva posible, estos Electrodos Pediátricos de Entrenamiento FR2 pueden usarse varias veces en cualquier maniquí de RCP; permitiendo a los alumnos recrear el proceso de rescate para ayudar a aumentar su confianza.

Los electrodos de formación son una herramienta de entrenamiento positiva para ayudar a los alumnos a entender la aplicación eficaz de los electrodos al tratar a una víctima de un paro cardiaco. Dado que la colocación de los Electrodos Pediátricos es diferente a la de los adultos en un rescate, estos electrodos de entrenamiento proporcionan una herramienta útil para entender la diferencia de los tratamientos.

Los electrodos se pueden utilizar tantas veces como sea necesario para demostrar el proceso de rescate, dando a los usuarios potenciales la oportunidad de ponerse manos a la obra con su DEA y practicar los pasos de rescate para ayudar a salvar una vida.

Utilizando los electrodos de entrenamiento de la misma manera que lo haría con los electrodos clínicos, los alumnos pueden practicar cómo aplicar los electrodos para realizar la desfibrilación más eficaz, que es vital para aumentar las posibilidades de supervivencia de una víctima.

Más Información

¿Quiere aprender más sobre los Electrodos Pediátricos de Entrenamiento FR2? Puede llamar a nuestro equipo en el  888 820 0760 el cual le aconsejará con gusto sobre cualquiera de nuestros productos para ayudarle a encontrar el equipo de formación adecuado que satisfaga sus necesidades.

 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.