Defibtech Lifeline VIEW/ECG/PRO 4 Year Replacement Battery Pack

Defibtech Lifeline VIEW/ECG/PRO 4 Year Replacement Battery Pack

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Defibtech Lifeline VIEW/ECG/PRO 4 Year Replacement Battery Pack

Product Code DCF-2003

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What's Included?

  • Lifeline VIEW/ECG 4-Year Replacement Battery Pack

Designed for use with the Defibtech Lifeline VIEW and ECG devices, this battery will provide 4 years of power to your life-saving device.

For use exclusively with the Defibtech Lifeline View and ECG, this replacement battery will provide 4-years of power to your unit and ensure it is ready for use during an emergency with a moment's notice.

Alongside being capable of delivering the life-saving treatment to a victim of sudden cardiac arrest, it is important that the AED can also carry out the required self-checks which ensure all the subsystems, accessories and software are in full working order.

Battery Features

  • Designed exclusively for the Lifeline View and ECG AEDs
  • Standby battery life of 4 years or the equivalent of 125 shocks/ 8 hours of continuous operating time
  • Ensures the AED can perform the daily self-checks
  • Lithium/Manganese Dioxide battery which is disposable and recycleable

How to Use

When changing your battery over, simply remove the old battery from the unit and install the new one. Once the battery has been inserted and the device has been switched on, your AED is ready for use. It's as simple as that. After successful insertion into the device, there is an integrity test carried out.

The battery ensures that everything required to carry out a rescue is in full working order and can be used during an emergency.

About the Manufacturer

Based in the United States, Defibtech have been innovating and manufacturing AEDs since 1999. Since day one they have designed a robust range of AEDs that have been tested and manufactured to a Military grade standard.

One of Defibtech's most notable achievements was back in 2006 where their Lifeline AEDs were selected to be part of the 2006 Winter Olympic Games in Torino, Italy and protect both spectators and athletes alike.

More Information

If you would like to learn more about the Defibtech Lifeline VIEW/ECG 4 Year Replacement Battery Pack, the friendly team at defibshop are here to help.

Call 800 989 7768 and one of our experts will be happy to answer any questions you may have.

 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.