ZOLL CPR-D padz Training Electrodes

ZOLL CPR-D padz Training Electrodes

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ZOLL CPR-D padz Training Electrodes

Product Code 8900-0804-01USA

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What's Included?

  • Electrodos CPRD Training 

Para usar con las unidades de formación Zoll, estos electrodos CPRD-Pad ayudaran a los usuarios a aprender la colocación de los electrodos más efectiva para ayudar a promover la desfibrilación más eficaz.

Modo de Empleo

Diseñados en su forma característica de 'Z', los usuarios pueden aplicar electrodos en un solo movimiento rápido, eliminando cualquier vacilación y ahorrando un tiempo valioso. Se puede usar una clavija incorporada para ajustar los electrodos y que se fijen correctamente en las víctimas de mayor estatura.

Si bien los electrodos clínicos deben reemplazarse después de cada uso, los Electrodos de Entrenamiento CPRD se pueden usar una y otra vez para demostrar la colocación de los electrodos más efectiva en una emergencia cardíaca. Al usar electrodos de entrenamiento, puede familiarizarse con la posición óptima de los electrodos, por lo que si alguna vez tiene que aplicarlos en un escenario de rescate real, puede hacerlo con facilidad y confianza.

Más Información

Para obtener más información sobre los Electrodos CPRD-Pad para las unidades de entrenamiento Zoll, puede llamar a nuestro amable equipo de Defibshop al 0000 000000.

Como proveedor completamente independiente de todos los productos DEA, puede estar seguro de que los consejos que le ofreceremos son totalmente imparciales y están diseñados para ayudarle a encontrar los productos perfectos para usted.

 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.