Physio Control LIFEPAK 15 NIBP Hose, 12'

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Physio Control LIFEPAK 15 NIBP Hose, 12'

Product Code 21300-008146USA

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What's Included?

  • LIFEPAK 15 NIBP Hose, 12'

Designed for use with Physio Control’s Lifepak 15 AED/ Monitor range, the LIFEPAK 15 NIBP Hose, 12' will enable you to connect an NIBP cuff to the device so the patient’s blood pressure can be taken. 

Unlike other AEDs, the Lifepak 15 AED/ Monitor range boasts a wide variety of medical grade features, including the ability to provide a blood pressure reading for a patient. Being able to provide a blood pressure reading can help determine any future treatment requirements for the patient.

About Physio Control

Since their launch in 1955, Physio Control has gone on to become one of the world’s most recognized AED manufacturers.

Their vision of no one person dying as a result of a treatable cardiac condition has led them on to continually develop their Lifepak AED range which can be traced back all the way to 1968 with the Lifepak 33 – more recently they’ve been noted for their development of the Lifepak CR Plus.

All AED devices designed by Physio Control are designed will all responder levels in mind, so regardless of whether you’re a trained professional or a first-time responder, you can feel confident in the life-saving treatment you’re delivering.

More Information

If you would like more information about the LIFEPAK 15 NIBP Hose, 12', the defibshop team are here to help.

To speak to one of our Product Specialists, call 888 820 0760 and one of our advisors will be happy to share their knowledge with you.

 

 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.