Physio Control LIFEPAK 1000 Pediatric Redipak Electrode Starter Kit

Physio Control LIFEPAK 1000 Pediatric Redipak Electrode Starter Kit

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Physio Control LIFEPAK 1000 Pediatric Redipak Electrode Starter Kit

Product Code 11101-000017USA

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What's Included?

  • Kit Inicio Electrodos Pediátricos Redipak para su uso con el Lifepak 1000

Para utilizar con la gama Lifepak 1000, los Electrodos Pediátricos Redipak permiten a los usuarios proporcionar una atención eficaz a niños menores de 8 años reduciendo automáticamente, a un nivel seguro, los julios administrados en la descarga. 

Lamentablemente, nadie es inmune a sufrir un paro cardíaco, incluidos los niños; por lo tanto, recomendamos mantener un conjunto de electrodos pediátricos con su DEA,  y así ser capaz de realizar con seguridad el tratamiento vital a cualquier víctima de PCS.

Características Electrodos

  • Uso exclusivo con el desfibrilador Lifepak 1000 de Physo Control
  • Reduce la salida de julios de la unidad a un nivel adecuado para un niño
  • Se proporcionan instrucciones claras, asegurando que los usuarios saben dónde colocar los electrodos antes del tratamiento
  • Tarjetas explicativas proporcionadas como parte del paquete de inicio para ayudar con la conexión de los electrodos

Modo de Empleo

Una vez conectados a su DEA, el nivel de julios administrados a través de los electrodos se reducirá automáticamente, asegurando que es seguro para el tamaño y la constitución de un niño.

Una vez los retire del envoltorio protector, aplique los electrodos al niño siguiendo las instrucciones y ayuda visual proporcionadas en los electrodos. Cuando se conecten, su DEA se pondrá inmediatamente a trabajar y analizará el ritmo cardíaco del paciente antes de determinar si se requiere desfibrilación.

Si detecta un ritmo cardiaco desfibrilable, el DEA proporcionará automáticamente una descarga si se trata de un dispositivo totalmente automático o le indicará que administre el choque presionando un botón si es Semiautomático. La RCP también será recomendada durante este tiempo.

Más información

Si desea obtener más información sobre los Electrodos Pediátricos y qué marca y producto son necesarios para su unidad DEA, póngase en contacto con el equipo defibshop.

Con años de experiencia a nuestras espaldas, puede confiar en que le podemos aconsejar qué producto es el más adecuado para su dispositivo. Para ponerse en contacto, llame al 888 820 0760.

 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.