LIFEPAK 12 NIBP Hose, 12'

LIFEPAK 12 NIBP Hose, 12'

Product Code 11996-000390

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What's Included?

  • LIFEPAK 12 NIBP Hose, 12'

For use with the Lifepak 12 from Physio Control, the LIFEPAK 12 NIBP Hose, 12' enables the user to connect the AED/ Monitor device to a NIBP cuff which can then be used to gather a blood pressure reading from the patient. 

Many AEDs can only be used in cardiac arrest emergencies whereas the Lifepak 12 from Physio Control boasts medical grade features, allowing more treatment options to be provided to the patient; one of these features being blood pressure readings.

Being able to gather information about the patient’s blood pressure will allow you to determine if any further treatment is required by the patient.

About Physio Control

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

This vision has allowed Physio Control to continually develop their Lifepak AED range which can be dated back to 1968 with the creation of the Lifepak 33 AED/ Monitor.

Since day one, all of Physio Control’s devices have been created with simplicity at the core of the design, allowing people of all response levels to confidently act if an emergency should arise.

More Information

If you would like to learn more about the LIFEPAK 12 NIBP Hose, 12' or any of the other Physio Control devices or accessories, the defibshop team are always here to help.

Get in touch with one of our advisors by calling 888 820 0760 and one of our team members will be happy to assist you in finding the perfect products for your needs and budget.

 

 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.