Philips OnSite Adult SMART Pad Cartridge Bundle (Pack of 2)

Philips OnSite Adult SMART Pad Cartridge Bundle (Pack of 2)

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Philips OnSite Adult SMART Pad Cartridge Bundle (Pack of 2)

Product Code M5071AbUSA

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What's Included?

  • Paquete Recambios SMART Pad para adultos HS1 (pack de 2)

Para utilizar con la gama de DEAs HS1 de Philips, el Recambio HS1 SMART Pad le asegurará que su DEA ofrece un rescate eficaz y con un repuesto a mano, siempre tendrá un respaldo.

Tener un juego de electrodos de repuesto con su DEA asegura que pase lo que pase, siempre estará preparado para actuar en caso de que alguien sea víctima de un paro cardiaco repentino.

Los minutos que siguen a que alguien sufra de un paro cardiaco súbito son vitales para su supervivencia. Si se utiliza un DEA dentro de los  3-5 minutos tras el colapso, sus oportunidades de sobrevivir aumentan del 6% al 74%! Tener los electrodos pre-conectados le ayudará a cerrar la brecha entre el colapso y la administración del tratamiento, dando una mayor probabilidad de sobrevivir a las víctimas.

Características principales

  • Diseñado específicamente para su uso con el DEA HS1 de Philips
  • Pre-conectados ayudando a ahorrar tiempo en una emergencia cardiaca
  • 2 años de vida útil hasta que los electrodos necesiten substitución
  • Sustancia conductora adhesiva que asegura que una vez que los electrodos estén colocados sobre la víctima, no se moverán durante el tratamiento

 

Modo de Empleo

El Recambio SMART Pad  Adultos HS1 está diseñado para ser pre-conectado antes de ser utilizado en una emergencia. Se pueden ahorrar minutos vitales durante este tiempo gracias a esta característica y el rescatador puede centrar su atención en el tratamiento del paciente.

Una vez que los electrodos se conectan correctamente a la víctima de un paro cardiaco, comenzarán a analizar su ritmo cardíaco y retransmitir los datos de nuevo al DEA. Esto ayudará a determinar si requieren una descarga del DEA o no.

Si se detecta taquicardia ventricular (VT) o fibrilación ventricular (VF) por parte del DEA, el dispositivo avisará que una descarga va a ser realizada, pero si no se detecta ninguno de estos ritmos cardíacos, el DEA no aconsejará el tratamiento.

 

Más información

Si tiene alguna pregunta sobre el Paquete de Recambio SMART Pad para Adultos HS1 de Philips, entonces el amable equipo experto defibshop está aquí para ayudarle.

Llámenos al 888 820 0760 y uno de nuestros asesores imparciales responderá con gusto a cualquier pregunta que pueda tener.

 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.