Laerdal Resusci Jr

Laerdal Resusci Jr

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Laerdal Resusci Jr

Product Code 18001001

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En existencia

What's Included?

  • Hard plastic Carry Case
  • Training Mat
  • Track Suit
  • 4 Junior Faces
  • 4 Junior Airways
  • 12 Manikin Wipes
  • Directions for Use

The lifelike Resusci Jr training manikin has been designed specifically to teach about child resuscitation and rescue methods.

The Resusci Jr training manikin offers a full-body construction that has been specifically designed to offer high-quality education about child CPR for your learners.

Students can quickly improve their skills and feel confident in performing CPR on a child in a real-life emergency.

Key Features

  • Realistic features
  • Head tilt and jaw thrust manouever
  • Realistic chest rise verifies ventilation
  • Anatomically correct
  • Disposable, non-rebreathing airways

About the Manufacturer

Laerdal started off back in 1940 as a small publishing house that specialized in children's books and greetings cards. Soon after they developed children's toys and eventually first aid manikins.

Fast forward to the present day, Laerdal are one of the world's most recognised first aid equipment manufacturers continually developing products that can assist with CPR training, airway management, AEDs and patient simulation.

More Information

If you would like to learn more about the Resusci Jr, the defibshop team are here to help.

Call 888 820 0760 to speak to one of our Product Specialists and they'll 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.