Philips FRx Carry Case

Philips FRx Carry Case

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Philips FRx Carry Case

Product Code 989803139251USA

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What's Included?

  • Maletín Trasporte FRx

Diseñado para su uso con la gama DEA FRx de Philips, este maletín de transporte protegerá y almacenará su DEA cuando este en movimiento.

El diseño rojo intenso y el símbolo universal de "AED" en el maletín ayudará a los transeúntes a identificar fácilmente el contenido del maletín, ayudando a reducir el tiempo entre la obtención del DEA y el tratamiento, en caso de que un paro cardiaco ocurra en la zona.

El asa de transporte adicional y la correa de hombro permiten que el DEA se transporte con facilidad, para que pueda llevar con seguridad la unidad a la escena de un rescate.

Modo de Empleo

Simplemente inserte su DEA Heartstart FRx en su nuevo maletín de transporte y ¡ya está listo! El maletín está diseñado para proporcionar una protección eficaz contra el polvo y el agua. Esto ayudará a asegurar que el equipo se mantenga en un estado de funcionamiento óptimo.

El maletín viene con un compartimento adicional que le permite almacenar electrodos y un kit de rescate. Almacenar el DEA y los accesorios necesarios juntos ayudará a acortar el tiempo entre el colapso de la víctima y el tratamiento administrado ya que todos los elementos esenciales necesarios están juntos y listos para ser utilizados.

El maletín contiene una ventana de manera que el indicador de estado es visible. Esto le ayudará a mantenerse al tanto del mantenimiento de su DEA y de si el dispositivo esta defectuoso, la batería baja o simplemente requiere atención, todo sin tener que sacar el dispositivo del maletín.

Más información

Si desea más información sobre el Maletín de Transporte FRx o cualquier otro producto listado en nuestro sitio web, el equipo defibshop está aquí para ayudarle.

Póngase en contacto llamando al 888 820 0760 y uno de nuestros amables asesores le ayudará de todas las maneras posibles.

 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.