NIBP Cuff Disposable, Infant

NIBP Cuff Disposable, Infant

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NIBP Cuff Disposable, Infant

Product Code 11160-000012

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What's Included?

  • NIBP Cuff-Disposable Infant

Designed for use with Physio Control’s Lifepak 15 and Lifepak 12 AED/ Monitor range, the infant NIBP Cuff will allow you to effectively measure an infant’s blood pressure. 

Unlike other AEDs that are only used for defibrillation of the heart in a cardiac arrest emergency, the Lifepak 12 and 15 boast extra features that enable the device to perform another medical practice’s on your patient.

By monitoring your patient’s blood pressure you’re providing professional medical care which can help determine future treatment requirements, if necessary.

About Physio Control

Since 1955, Physio Control has been working towards a vision in which no one person dies as a result of an acute, treatable cardiac emergency.

This vision has led the company to become one of the world’s most well-known AED designers and manufacturers. One of their most notable creations is the Lifepak CR Plus AED range.

All devices created by Physio Control have ease of use and simplicity at the heart of the design. This ideology enables rescuers of all levels to effectively provide the potentially life-saving care required by the victim of sudden cardiac arrest with confidence.

More Information

If you would like to learn more about the NIBP Cuff-Disposable Infant or any other product listed on our website, get in touch with the defibshop team.

Call 888 820 0760 and one of our friendly, expert advisors 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.