Physio Control CR Plus CHARGE-PAK Charging stick and two sets of Quickpak electrodes

Physio Control CR Plus CHARGE-PAK Charging stick and two sets of Quickpak electrodes

Imagenes Adicionales

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Physio Control CR Plus CHARGE-PAK Charging stick and two sets of Quickpak electrodes

Product Code 11403-000001USA

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What's Included?

  • Cargador CHARGE-PAK
  • dos sets de Electrodos Quickpak

Para uso con el DEA Lifepak CR Plus de Physio Control, la batería CHARGE-PAK ™ y los electrodos Quickpak garantizan que su DEA esté siempre listo para salvar una vida.

Esta combinación de cargador de  batería y dos juegos de electrodos está diseñado para su uso con la gama Lifepak CR Plus de Physio Control. Gracias al reemplazo conjunto de ambos accesorios vitales cada dos años, el mantenimiento de este DEA no podría ser más fácil o más eficiente.

Tener un juego de electrodos de repuesto es algo que siempre recomendamos. Elimina la presión del usuario al colocarlos correctamente por primera vez. Si no tienen éxito, estos electrodos no pueden ser reutilizados, mientras que tener un segundo juego electrodos aún le da la oportunidad de ayudar a salvar una vida.


• Vida útil de la batería de 2 años

• Vida útil de los electrodos de 2 años

Modo de Empleo

Simplemente conecte los electrodos al DEA a través de los cables e instale la batería en la parte correspondiente.

Los electrodos se pueden almacenar debajo de la tapa antes de usarlos para mantenerlos seguros. El Lifepak CR Plus realizará una autocomprobación una vez encendido para asegurarse de que los accesorios se han instalado y conectado correctamente y que el DEA está listo para su uso.

Más Información

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 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.