AED Pro Battery Recharger


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AED Pro Battery Recharger

Product Code 8050-0030-01USA

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En existencia

What's Included?

  • Cargador AED Pro

Este cargador garantizará que su batería recargable AED Pro esté completamente cargada en todo momento para asegurarse de que puede realizar un rescate cuando sea vital.

Usted puede gestionar fácilmente el mantenimiento de su desfibrilador cargando su batería como y cuando lo necesite para que pueda ser utilizado con éxito al realizar la desfibrilación a una víctima de paro cardiaco.


  • Función carga rápida
  • Prueba de fallos


Modo de Empleo

Se recomienda que mantenga la batería completamente cargada en todo momento, de manera que pueda trabajar a su máximo potencial si alguien sufre un paro cardiaco.

Gracias a sus autocomprobaciones diarias, semanales y mensuales, su DEA le notificará cuando los niveles de la batería se están agotando a través de una alarma sonora, lo que le permite recargar la batería para que esté lista para utilizarse en caso de emergencia.

Hay varios controles de funcionamiento que indicarán si el cargador está funcionando correctamente y cuando la batería está completamente cargada y lista para ser instalada.

  Por ejemplo, para reconocer si la batería se ha insertado correctamente en el cargador, el indicador de "charger on" se iluminará.

Más Información

¿Quiere preguntar algo sobre el Cargador de Batería AED Pro? Nuestro equipo experto defibshop está a mano para ayudar. Llame al 00000 000000 para hablar directamente con nuestro equipo el cual contestará a cualquier pregunta que pueda tener.

 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.