Wall Mount Bracket for Lifepak 1000 and Lifepak 500

Wall Mount Bracket for Lifepak 1000 and Lifepak 500

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Wall Mount Bracket for Lifepak 1000 and Lifepak 500

Product Code 11210-000001USA

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What's Included?

  • Soporte de Montaje en Pared para Lifepak 1000 y Lifepak 500

Diseñado para utilizarse con los DEA Lifepak 1000 y Lifepak 500 de Physio Control, este soporte de pared asegura que su DEA esté a salvo, seguro y fácil de alcanzar en caso de una emergencia.

El Soporte de Montaje en Pared para Lifepak 1000 y Lifepak 500 garantiza que su DEA sea altamente visible para todos en el área mientras permanece bien protegido y es fácil de alcanzar  para que el DEA se pueda llevar rápidamente a la escena de emergencia, acortando el tiempo entre el colapso de la víctima y la desfibrilación.

Modo de Empleo

Cuelgue su Soporte de Montaje en Pared en el interior, en un lugar accesible y central para transeúntes y miembros del personal. Tener el dispositivo visible ayudará tanto a los transeúntes como al personal a familiarizarse con la ubicación del DEA, de modo que si alguien resultara víctima de un paro cardíaco, sabrá dónde se encuentra el DEA, lo que permite un alcance y tratamiento rápido.

La correa incorporada proporciona a su DEA una seguridad adicional, asegurando que esté protegido mientras está expuesto.

Más Información

Si desea obtener más información sobre el Soporte de Montaje en Pared para los DEA Lifepak 1000 y Lifepak 500, no dude en ponerse en contacto con uno de nuestros amables asesores.

Nuestros asesores expertos son los que tienen todas las respuestas a sus preguntas. Puede contactar directamente en el 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.