Defibtech Lifeline Demonstration Video

Defibtech Lifeline Demonstration Video

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Defibtech Lifeline Demonstration Video

Product Code DAC-520-V1

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What's Included?

  • Defibtech Lifeline Demonstration Video

Want to get to know your new Defibtech Lifeline AED? This demonstration video has been created to highlight the important features built-in to your Lifeline unit, so you can have a better understanding in the operational functions of your AED device.

Confidence is Key

When providing care to a victim of cardiac arrest, confidence in the treatment your delivering is vital for an effective rescue. Knowing exactly how your AED functions and what you can expect from its features will help to increase your ability in using the device, giving you a better understanding of what to expect when you come to use the device for a rescue.

To further your knowledge and confidence, we also advise CPR and AED training to complement this product. Training will allow you to get hands-on with your AED to better understand how it operates while CPR will help you to provide the most effective compressions possible to increase a patient’s chances of survival.

More information

Do you have a question for a member of our team? Whether you require further information about this product, or would like to learn more about a particular AED, our AED Product Specialists are on hand to take your call.

Contact 000000 000000 or email savealife@thedefibshop.com for more information.

 

 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.