FilterLine Set Long Adult/Pediatric (box of 25)

FilterLine Set Long Adult/Pediatric (box of 25)

Product Code 11996-000164

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What's Included?

  • FilterLine Set Long Adult/Pediatric (box of 25)

Designed for use with the Lifepak 12 AED/ Monitor range, the FilterLine Set Long Adult/ Paediatric (box of 25) will allow you to provide the most effective care for both adult and paediatric patients that require monitoring. 

These tubes can be used with the Lifepak 12 EtCO2 Adult/ Paediatric circuit on patients that require intubation for a short term of time – typically 24 hours. Includes airway adapter.

About Physio Control

Physio Control has envisioned a society in which no one person dies as a result of a treatable, cardiac event since their launch back in 1955. This vision has led them on to develop the Lifepak AED range which began with the Lifepak 33 AED/ Monitor in 1968.

As time has passed, the continual developments of the Lifepak AED range have made life-saving treatment simplistic and hassle-free. Each and every device designed and manufactured by Physio Control is designed with both trained and non-trained users in mind, allowing almost anyone to react with confidence in an emergency.

More Information

If you would like more information about the FilterLine Set Long Adult/Pediatric (box of 25), the defibshop team are here to help.

To speak to one of our advisors, simply call 888 820 0760 and they’ll be happy to assist you in any way they can.


 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.