CHARGE-PAK Charging stick and one set of Quickpak electrodes

CHARGE-PAK-Charging-stick-one-set-Quickpak-electrodes

Imagenes Adicionales

  • CHARGE-PAK-Charging-stick-one-set-Quickpak-electrodes
  • CHARGE-PAK-for-use-with

CHARGE-PAK Charging stick and one set of Quickpak electrodes

Product Code 11403-000002USA

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What's Included?

 

  • Cargador  CHARGE-PAK
  • un juego de Electrodos Quickpak

 

El mantenimiento del DEA es clave para asegurar que su unidad esté preparada para rescate y sea capaz de realizar una descarga a una víctima de un paro cardiaco. El reemplazo de los electrodos y la batería hace que el mantenimiento sea aún más sencillo.

El CHARGE-PAK le ofrece la posibilidad de reemplazar los electrodos y la batería al mismo tiempo, dándole confianza de que su dispositivo estará siempre listo para su uso en cualquier momento.

El cargador de batería proporcionará suficiente energía para 25 descargas adicionales, mientras que los electrodos nuevos le proporcionarán más adhesivo conductor asegurando que el contacto con la piel de la víctima es seguro.

Características

• Vida útil del cargador de batería de 2 años

• Vida útil de los electrodos de 2 años

Modo de Empleo

Cuando los niveles de su batería original sean bajos, este paquete le proporcionará a su DEA energía adicional.

Simplemente instale la batería nueva y conecte los electrodos. El DEA realizará automáticamente una autocomprobación una vez que se haya encendido. Una vez que esto se haya completado, el DEA debe estar listo para la acción.

Si le preocupa que el DEA funcione correctamente, el indicador de estado le avisará si el dispositivo requiere atención. Estas notificaciones se realizan con la aparición de un pequeño símbolo de una llave inglesa y también podrían usarse avisos de audio.

Recomendamos no abrir la tapa del DEA hasta que sea necesario en un rescate. Al levantar la tapa, el dispositivo entrará automáticamente en modo de desfibrilación, lo que puede hacer que la batería se vacíe.

Más Información

Si desea obtener más información sobre el cargador CHARGE-PAK o los electrodos Quickpak, póngase en contacto con el equipo defibshop.

Simplemente llame al 0000 000000 y uno de nuestros asesores estará encantado de ayudarle

 

 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.