Product Code 8000-0838

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What's Included?

  • Cable 3 Derivaciones ECG AED Pro 

Diseñado para uso exclusivo con el Zoll AED Pro, este cable de 3 derivaciones ECG permite a los usuarios ver los datos de ECG almacenados en el dispositivo, tras un suceso de paro cardiaco.

Este accesorio es un accesorio práctico de su desfibrilador que permite a los servicios de emergencia y al personal del hospital  ver los datos de rescate después de que se haya llevado a cabo, de manera que se puedan administrar los cuidados post-cardiacos más efectivos.

Acerca del Fabricante

El desarrollo de equipamientos médicos Zoll se remonta al año 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.

Este accesorio puede ayudar a administrar a las víctimas los cuidados posteriores apropiados basándose en el rescate antes realizado. Los datos pueden ser transferidos instantáneamente usando el cable ECG y vistos por profesionales que podrán ver exactamente cuántas descargas fueron realizadas y  con qué fuerza, lo que les permite hacerse una imagen de todo el proceso de rescate.

Más Información

¿Tiene alguna pregunta sin contestar respecto al cable 3 Derivaciones ECG AED Pro? Entonces es mejor que llame al equipo defibshop.

Como expertos en todo lo relacionado a los DEA y como proveedor independiente, podremos proporcionarle todas las respuestas que necesita mientras le ayudamos a encontrar el equipo adecuado para sus necesidades, para ponerse en contacto llame al 0000000 00000 0000.

 

 

 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.