Cardiac Science Powerheart G3 AED semi-rigid carry case w/strap and back storage compartment

Cardiac Science Powerheart G3 AED semi-rigid carry case w/strap and back storage compartment

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Cardiac Science Powerheart G3 AED semi-rigid carry case w/strap and back storage compartment

Product Code 168-6000-001USA

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What's Included?

  • Bolsa Transporte para Gama G3 de Powerheart 

¿Está buscando proteger su DEA G3 Cardiac Science durante su transporte? Esta bolsa de transporte semirrígida ha sido diseñada teniendo en cuenta la funcionalidad, por lo que puede llevar su dispositivo de salvamento a donde quiera que vaya.

Con un asa de hombro ajustable para facilitar el transporte y ventanas visibles de manera que es capaz de comprobar el indicador de “rescate listo” y las fechas de caducidad de los electrodos sin ni siquiera sacar la unidad de la bolsa, puede tener confianza en todo momento de que su DEA está listo para el rescate y disponible en caso de una emergencia cardiaca.

Modo de Empleo

La bolsa ha sido diseñada con un bolsillo grande en la parte trasera, lo que le proporciona un amplio espacio para almacenar sus accesorios esenciales, como electrodos, kit de rescate y baterías de repuesto. Al mantener sus accesorios juntos en un único lugar, puede estar seguro de que siempre puede utilizarlos a su máximo potencial, en caso de que alguien sufra un paro cardiaco.

Al mantener sus accesorios cerca, puede ahorrar minutos vitales en un escenario de rescate donde el tiempo lo es todo. Con cada minuto que pasa, la probabilidad de supervivencia de una víctima de un paro cardíaco disminuye en un 10%, por lo que el acceso rápido a su DEA y consumibles es esencial para dar a la víctima las mejores posibilidades de supervivencia.

Más Información

¿Quieres saber más sobre la Bolsa de transporte Powerheart G3 antes de comprar? Nuestros asesores defibshop son a los que llamar.

Con una amplia experiencia en la industria de DEA, podremos proporcionarle consejos honestos e imparciales para ayudarle a encontrar el producto adecuado para usted. Para ponerse en contacto, simplemente llame 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.