Product Code DCU-E2301ENUSA

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What's Included?

  • Tarjeta Demostración Lifeline View

Para usar con el DEA de Defibtech Lifeline View, los usuarios pueden usar esta tarjeta de demostración para practicar usando su unidad de salvamento en "modo demostración". Esto permitirá a los usuarios potenciales conocer su unidad de una manera más relajada, de manera que serán capaces de actuar con confianza en el caso de un paro cardiaco.

Modo de Empleo

Puede insertar y quitar la tarjeta de demostración siempre que quiera, lo que le permite utilizar el DEA Defibtech Lifeline View en modo de entrenamiento tan a menudo como lo desee. Esto favorece a proporcionar un escenario de entrenamiento realista una y otra vez, para ayudar a aumentar la confianza del usuario y el conocimiento sobre las características exclusivas de su dispositivo.

Si se produce una emergencia cardiaca mientras se inserta la tarjeta de demostración, puede cambiar rápidamente su DEA, de nuevo al modo clínico, rápida y fácilmente para realizar un rescate.

Más información

¿Desea obtener más información sobre la Tarjeta de Demostración Lifeline View? El equipo defibshop está a su disposición para atender su llamada.

Nos gusta pensar que estamos suficientemente bien informados cuando se trata de DEAs, después de haber estado en la industria durante más de una década. Puede ponerse en contacto llamando al 0000 0000000 donde un miembro de nuestro equipo estará encantado de ayudarle con cualquier pregunta.

 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.