Physio Control Lifepak 15 Lithium Ion Battery 5.8 Ah

Physio Control Lifepak 15 Lithium Ion Battery 5.8 Ah

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Physio Control Lifepak 15 Lithium Ion Battery 5.8 Ah

Product Code 21330-001176USA

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What's Included?

  • Batería de Ion-Litio 5.8 Ah  Lifepak 15 

El Lifepak 15 de Physio Control soporta dos baterías de Iones de Litio con tecnología de batería dual, lo que permite al usuario cambiar de una fuente de alimentación a la otra con facilidad. La resistencia de este DEA ayuda a la batería a soportar los factores más severos, como impactos, altas temperaturas y humedad.

Modo de Empleo

Esta batería se puede cargar una vez instalada en su DEA, utilizando un adaptador de CA o CC. El tiempo de carga normal es de 190 minutos.

Para asegurarse de los niveles actuales de la batería, simplemente observe el indicador de nivel de energía y / o si es visible el mensaje de "low battery". Una vez que la energía de la batería haya alcanzado un nivel críticamente bajo, un mensaje de audio sonará indicando “replace battery” y el dispositivo cambiará automáticamente a la batería alternativa.

Los usuarios pueden rastrear la función y la duración restante de sus baterías utilizando la red de sistema de datos LIFENET.

La fuente de alimentación permite al DEA desfibrilar al paciente si se requiere. Esta descarga será de energía escalonada, hasta una dosis de alta-energía de 360 ​​Julios.

 

Acerca del fabricante

Physio Control aspira a crear una sociedad en la que nadie muera a causa de una condición médica tratable.

Su tecnología ha sido diseñada con la facilidad de uso principalmente, lo que permite a los profesionales médicos y a los usuarios no capacitados tratar con confianza el paro cardiaco repentino.

Physio Control ha estado funcionando durante más de 55 años y se han convertido en uno de los fabricantes más conocidos del mundo de DEAs que salvan vidas.

 

Más información

Si desea más información sobre la Batería Ion-litio de Lifepak 15, el equipo defibshop es el que tiene todas las respuestas.

Simplemente llame al 888 820 0760 y uno de nuestros asesores imparciales le ayudará en todo lo que necesite.

 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.