Product Code 11140-000074USA

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What's Included?

  • Adaptador CC Lifepak 15

Este Adaptador de corriente continua (CC) Lifepak 15 le permitirá cargar su DEA de una fuente de corriente eléctrica directa, eliminando la necesidad de remplazar las baterías. 

Características

  • Desconexión rápida
  • Carga constante                                                                                              

Modo de Empelo

Ideal para entornos clínicos donde la unidad podría usarse regularmente, el Adaptador de CC Lifepak 15 es un dispositivo portátil y proporciona suficiente carga al Lifepak 15 cuando se conecta a una fuente de corriente eléctrica directa. El adaptador se puede conectar a las tomas de corriente dentro de los vehículos de los EMS, por lo que los médicos que se dirigen a una emergencia son capaces de mantener su unidad totalmente cargada y preparada.

El adaptador se puede montar tanto en carros de parada como en las paredes de un hospital para garantizar que el tratamiento se puede realizar rápidamente si se requiere. El adaptador se puede desconectar fácilmente y puede transportar el DEA al lugar donde sea necesario para ayudar a salvar una vida.

Más información

Si tiene alguna pregunta respecto al Adaptador CC Lifepak 15, nuestros especialistas en producto están a tan sólo una llamada de distancia.

Puede ponerse en contacto llamando al 000000 00000 o enviando sus preguntas a savealife@thedefibshop.com donde un miembro de nuestro equipo 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.