Laerdal Resusci Jr Water Rescue

resusci-jr-water-rescue

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Laerdal Resusci Jr Water Rescue

Product Code 18001201

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In Stock

What's Included?

  • Full Body Pediatric Manikin
  • Carry Case
  • Training Mat
  • Water Rescue Kit
  • Track Suit
  • 4 Junior Faces
  • 4 Junior Airways
  • 12 Manikin Wipes
  • Directions for Use

The Resusci Jr training manikin has been designed to educate trainers on the correct techniques for treating a child in need of CPR.This specific package includes the water rescue kit which provides learners with the opportunity to experience life-like water rescue techniques.

The Resusci Jr Water Rescue allows students to experience a life-like water rescue technique, so if a child should need rescuing in water, your trainees will know how to act, with confidence.

Key Features

  • Anatomically correct
  • Can be used in water
  • Realistic chest rise to show correct ventilation
  • Realistic resistance for chest compressions
  • Head tilt and jaw thrust manoeuvres

About the Manufacturer

Laerdal are one of the world's leading manufacturers that specialize in the development of first aid products that cater for CPR training, airway management, AEDs and patient simulation.

Did you know they started off as a small publishing house that specialized in children's books and greetings cards in 1940?

More Information

If you would like to learn more about the Resusci Jr Water Rescue, the defibshop team are on hand to assist.

Call 800 989 7768 to speak to one of our expert advisors and they'll be happy to help 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.