Product Code 05-10100

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What's Included?

  • Aadaptador Electrodos para Zoll

Un accesorio práctico si se encuentra con electrodos incompatibles, este adaptador de electrodos conectará electrodos de otras marcas a cualquier desfibrilador Zoll.

En una situación de emergencia, usted desea tener las herramientas para realizar con éxito la atención a una víctima de un paro cardiaco, tener este adaptador a la mano facilitará cualquier preocupación que pueda tener y le permitirá desfibrilar una víctima, incluso si sus electrodos y DEA no combinan correctamente.

Acerca del fabricante

El desarrollo de equipamiento médico Zoll se remonta a la década de 1950, cuando el doctor Paul Zoll comenzó a demostrar los efectos del desfibrilador externo en la creación de ritmos cardíacos estables después de sufrir un paro cardiaco.

Desde entonces, Zoll ha producido algunos de los DEAs más reconocibles en el mercado, especialmente el AED Plus. Brillante y destacado color, Zoll crear unidades llamativas equipadas con tecnología avanzada para permitir a los usuarios, con cualquier nivel de experiencia, la capacidad de utilizarlos con confianza en caso de una emergencia.

Más información

¿Tienes alguna pregunta sin respuesta sobre el Adaptador de Electrodos para los DEA Zoll? Nuestros amables y bien informados asesores están a su disposición para ayudarle.

Simplemente llame al 00000 0000000 y un miembro del equipo defibshop le ayudará con cualquier consulta 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.