Physio Control Lifepak 15 Redi-Charge Battery Adapter Tray

Physio Control Lifepak 15 Redi-Charge Battery Adapter Tray

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Physio Control Lifepak 15 Redi-Charge Battery Adapter Tray

Product Code 11140-000052USA

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What's Included?

  • Bandeja Adaptador Batería Redi-Charge Lifepak 15 

Esta estación de carga le permitirá mantener su unidad Lifepak 15 completamente cargada y poder ser utilizada en un rescate una y otra vez.

Sin una fuente de alimentación completamente cargada, su DEA no se puede usar para ayudar a salvar la vida de una víctima de paro cardíaco. Esta es la razón por la que esta Bandeja Adaptador de Batería Redi-Charge Lifepak 15 es un accesorio esencial a su kit para garantizar que la batería nunca esté baja de energía.

Modo de Empleo

El DEA Lifepak 15 requiere 2 baterías de Iones de Litio compatibles y recargables, la Bandeja Adaptador de Batería Redi-Charge, así como la Base Redi-Charge LifeLak 15 y un cable de alimentación de CA.

Una vez que la Bandeja Adaptador se encaja en la Base, las baterías pueden insertarse en la ranura adecuada. Con un tiempo de carga de aproximadamente 4.2 horas, la combinación de estos productos le permite mantenerse al día con el mantenimiento de su DEA Lifepak 15 para mantener su unidad constantemente cargada y preparada.

Más Información

¿Cree que la Bandeja Adaptador Batería Redi-Charge Lifepak 15 podría ser el producto adecuado para usted? Si tiene alguna pregunta o desea obtener más información antes de realizar la compra, contacte con el equipo de defibshop llamando al 888 820 0760.

 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.