Product Code DTR-201

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En existencia

What's Included?

  • Cargador Batería Entrenamiento

Para usar con el DEA de Formación Lifeline de  Defibtech, este cargador asegurará que su unidad de capacitación esté siempre cargada y lista para enseñar y formar a nuevos rescatistas.

Aunque se están diseñando, fabricando y colocando DEA de acceso público, más modernos en diversos entornos públicos, la formación en DEA garantiza que pueda usar los dispositivos con confianza. Tener conocimientos de primeros auxilios y DEA de primera mano solo mejorará la calidad de la atención médica salva vidas, que se proporciona a la víctima de un paro cardíaco.

Los minutos que siguen a un paro cardíaco son cruciales y con el entrenamiento, usted podrá ofrecer a la víctima las mayores posibilidades de sobrevivir. Si el tratamiento se administra exitosamente al paciente dentro de los 3-5 minutos tras el colapso, las posibilidades de supervivencia aumentan del 6% al 74%.

Características Principales

  • Diseñado para ser utilizado con el DEA de Formación Lifeline de Defibtech
  • Asegura que la batería de su unidad de capacitación siempre esté cargada y lista para formar a los alumnos

Más información

Si desea obtener más información sobre el Cargador de Baterías de Entrenamiento de Defibtech o simplemente tiene alguna otra pregunta acerca de los DEA o consulta sobre otros productos en nuestro sitio web, el amable equipo de defibshop está aquí para ayudarle.

Para hablar con uno de nuestros asesores expertos, simplemente llame al 0000 000000 y estarán encantados de ayudarle con sus preguntas.

 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.