Laerdal Little Anne


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Laerdal Little Anne

Product Code 120-01050USA

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In Stock

What's Included?

  • Little Anne Manikin
  • Soft Pack/Training Mat
  • 2 Manikin Faces
  • 2 Airways
  • 6 manikin wipes
  • User Guide
  • Jacket

The Little Anne training manikin helps trainers to provide the most realistic training first aid experience for their students. Future responders can practice each and every step of the rescue process, including CPR and administering treatment from an AED, so if a real-life emergency did occur, they would be able to provide the most effective care for the patient, with confidence.

Robust and lightweight, the Little Anne training manikin allows trainers to provide an effective training experience for their learners without having to compromise on quality.

The Little Anne will help ensure that by the of the training session, your student will know what is required of them during a cardiac emergency so they can act with confidence.

Key Features

  • Realistic airway construction
  • Head tilt feature emulates a realistic head tilt to provide mouth-to-mouth
  • Anatomically correct torso
  • Compatible with Laerdal's CPRmeter to enhance the training experince and receive real-time feedback
  • Ergonomic disposable airways for quick and easy clean-up after the session
  • Removable and reusable faces
  • Optional clicker feature which helps to acheive the correct chest compression depth
  • Lightweight design

About the Manuacturer

Originally starting out as a small publishing house, specializing in greetings cards and children's books. From there, Laerdal went on to develop children's toys which eventually led to them developing first aid manikins.

Since then, Laerdal have become one of the world's most well recognised medical technology developers, as they've dedicated their time to developing life-saving products, ranging from AEDs all the way to patient simulation.

More Information

If you would like more information about the Little Anne, the defibshop team are here to help.

Call 800 989 7768 and one of our team members will be happy to assist you in any way they can.

 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.