FilterLine Set Adult/Pediatric (box of 25)

FilterLine Set Adult/Pediatric (box of 25)

Product Code 11996-000081USA

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What's Included?

  • FilterLine Set Adult/Pediatric (box of 25)

Compatible with the Lifepak 12 AED/ Monitor, the FilterLine Set Adult/Pediatric (box of 25) will allow you to provide intubated care for adult and paediatric patients. 

For use with Intubated Applications by Physio Control, these tubes are fitted with an airway adapter for usage and are for use on short-term patients – typically 24 hours.

About Physio Control

Dating back to 1955, Physio Control introduced their life-saving device, the Lifepak 33 AED/Monitor thirteen years after their launch in 1968.

Since day one they have been working towards a vision of a society in which no one person dies of an acute, treatable cardiac condition. This vision has led them to continue developing the Lifepak AED range.

The creation of the Lifepak CR Plus is one of Physio Control’s most notable launches as it is now one of the world’s most recognized AEDs. Catering for both trained and untrained users, almost anyone can act in an emergency situation with confidence.

More Information

If you would like to learn more about the FilterLine Set Adult/Pediatric (box of 25), speak to one of our friendly advisors.

We pride ourselves on offering expert, impartial advice to help you find the perfect product for your needs and budget.

To speak to one of our advisors, call 888 820 0760 and they’ll be happy to help 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.