HeartStart FR2+ Toolkit, NTSC

HeartStart FR2+ Toolkit, NTSC

Product Code 9.89803E+11

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What's Included?

  • Batería FR2 

Diseñada para uso con el DEA Philips Heartstart FR2, esta batería permite a su DEA realizar un mínimo de 300 descargas cuando se instala inicialmente.

Uno de los aspectos más importantes de un DEA es su batería. Sin esta, el DEA no sería capaz de realizar una descarga que salva vidas o realizar las autocomprobaciones esenciales que ayudan a asegurar que su DEA está siempre en condición de rescate.

Tener una batería de repuesto para su DEA FR2 es algo que siempre recomendamos. Si su batería actual está cerca de expirar o el DEA se ha utilizado en un rescate, con una batería de repuesto se asegurará de que su DEA siempre se puede utilizar en una emergencia cardíaca.

Características Batería

  • Diseñada para uso exclusivo con la gama de Philips FR2 AED
  • Batería desechable de dióxido de litio-manganeso
  • 5 años de vida útil
  • Vida útil en stand-by de 5 años
  • Un mínimo de 300 descargas proporcionadas

Modo de Empleo

Simplemente inserte su nueva batería en el compartimiento correspondiente de su FR2 y su DEA estará listo para su uso. Esta batería de recambio proporcionará al DEA suficiente energía en modo stand-by durante 5 años, si no se utiliza en un rescate durante este tiempo.

El DEA llevará a cabo pruebas diarias de mantenimiento que ayudan a asegurar que todos los componentes del DEA, incluyendo los electrodos están en buen estado de funcionamiento, listos para ser utilizados en un rescate.

Más Información

Si desea obtener más información acerca de la Batería Philips FR2, el equipo defibshop, amable y bien informado, esta siempre a su disposición.

Llámenos al 0000 000000 y uno de nuestros asesores contestará gustosamente a cualquier pregunta 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.