Airway complete (pkg.96)
Airway complete (pkg.96)
Product Code 020301USA
- Airway Complete (pkg. 96)
Designed for use with Laerdal's Little Anne training manikin, the Airway Complete help to simulate air entering the lungs during mouth-to-mouth CPR.
This pack includes 96 non-rebreathing airways with a one-way valve. These airways should be changed after each class for maximum instructor convenience and student safety.
About the Manufacturer
Laerdal started their journey in a small publishing house that specialized in children's books and greetings cards. Soon after, they started to develop children's toys which led to them developing first aid manikins.
Fast forward to the present day and Laerdal is one of the world's most recognized medical equipment manufacturers. They continually dedicate their time to developing and manufacturing life-saving equipment, including patient simulation aids, AEDs, airway management aids and CPR training aids.
If you would like to learn more about the Airway Complete (pkg.96) from Laerdal, speak to one of the friendly experts, here at defibshop.
Call 888 820 0760 and one of our AED Product Specialists will be happy to assist you and provide all the answers you need.
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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.