Stabilization Strap (4 pack)

Stabilization Strap (4 pack)

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Stabilization Strap (4 pack)

Product Code 21576-000075

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What's Included?

  • Stabilization Strap (4 pack)

Designed for use with the LUCAS Mechanical CPR device, this strap enables the user to fully stabilize the patient, ensuring that they are in place and ready to receive the effective CPR from the device.

In this pack, you will be provided with 4 stabilization straps to use on patients who require effective CPR from the LUCAS device.

The LUCAS mechanical CPR device has been designed to allow responders to fully concentrate on the patient who may require a life-saving shock by performing effective CPR without hesitation.

Effective CPR is a key factor when treating a victim of sudden cardiac arrest and it is of vital importance that the patient receives effective CPR to provide them with the highest chance of survival.

About Physio Control

Physio Control are a world leader in the development and manufacturing of life-saving devices for both professionals and untrained responders.

All devices developed by Physio Control are equipped with professional-grade technology and easy to use interfaces, enabling users of all response levels to use the life-saving devices with the utmost confidence.

More Information

If you would like to learn more about the Physio Control Stabilization Strap (4 pack), the team here at defibshop are on hand to help.

To speak to one of our friendly experts, simply call 888 820 0760 and one of our Product Specialists 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.