Philips FRx Training Pads (replacement)

Philips FRx Training Pads (replacement)

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Philips FRx Training Pads (replacement)

Product Code 989803139291USA

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What's Included?

  • Electrodos de Entrenamiento FRx (reemplazo)

Para su uso con el DEA de Formación FRx, estos Electrodos de Entrenamiento ayudarán a los alumnos a entender la colocación de los electrodos más beneficiosa para una desfibrilación efectiva.

Mientras que cada paso del proceso del rescate es vital, la colocación de los electrodos es fundamental para ayudar a éstos a analizar el corazón del paciente en busca de un ritmo desfibrilable  y a realizar la desfibrilación si fuera necesario, para ayudar a salvar una vida.

El uso de electrodos de entrenamiento permitirá a los estudiantes practicar estos pasos vitales y experimentar escenarios de entrenamiento realistas, aumentando la confianza y la capacidad de proporcionar un rescate en caso de un paro cardiaco.

A diferencia de los electrodos clínicos, estos Electrodos de Entrenamiento FRx se pueden utilizar varias veces en un maniquí, para poder practicar y completar la cadena de supervivencia tantas veces como sea necesario. Una vez colocados en el maniquí, su unidad de entrenamiento pasará a la siguiente etapa del proceso de desfibrilación, como si fuera un verdadero rescate.

Más información

¿Tiene una pregunta sobre nuestros Electrodos de Entrenamiento FRx? El equipo defibshop está a su disposición para ayudar. Llame al 888 820 0760 donde podrá hablar con uno de nuestros asesores directamente para ayudarle a encontrar el producto adecuado para usted.

 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.