ZOLL AED Plus/Pro Pediatric Pedi Padz II - Single

ZOLL AED Plus/Pro Pediatric Pedi Padz II - Single

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ZOLL AED Plus/Pro Pediatric Pedi Padz II - Single

Product Code 8900-0810-01USA

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En existencia

What's Included?

  • Paediatric Pedi-Padz (1)

Los electrodos pediátricos son un elemento vital a mantener junto a su DEA para asegurarse siempre de poder rescatar a una víctima de un paro cardiaco, sin importar su edad.

Tristemente, el paro cardiaco le puede ocurrir a cualquier persona de cualquier edad, por lo que han desarrollado electrodos pediátricos específicos que automáticamente reducen el nivel de descarga a uno que es seguro para un niño entre las edades de 1-8 años.

La descarga habitual de 150 julios se reduce automáticamente a un nivel seguro a través de los electrodos, todo lo que tiene que hacer es conectarlos como lo haría con los electrodos regulares y comenzar el rescate.

Características Electrodos:

  • Para uso en niños de entre 1 y 8 años de edad.
  • Los electrodos pediátricos administran niveles más bajos de energía para proteger a los niños de posibles daños
  • Electrodos pre-conectados para ahorrar segundos valiosos
  • Diagramas claros y sencillos
  • Electrodos duraderos que caducan después de 18-24 meses.

Modo de Empleo

Retire los electrodos del embalaje siguiendo las indicaciones visuales del paquete. Colocar en el pecho desnudo del niño y en el centro de la espalda como se indica en las instrucciones. El DEA analizará entonces el ritmo cardíaco del niño y producirá un choque con niveles más bajos de energía que los electrodos para adultos, si es necesario.

Más información

¿Quieres saber más sobre el Paediatric Pedi Padz? Nuestros asesores expertos de defibshop son a los que debe llamar.

Marque 888 820 0760 y contactará directamente con defibshop.

 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.