Laerdal Baby Anne


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  • baby-anne

Laerdal Baby Anne

Product Code 130-01050USA

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What's Included?

  • 1 Baby Anne Manikin
  • Soft Pack
  • 6 Airways
  • 10 Foreign Body Practice Objects
  • Directions for Use

The Baby Anne manikin will enable trainers to teach their students how to effectively treat a baby in an emergency situation.

The Baby Anne training manikin helps students to understand what needs to be done when a baby requires first aid or CPR. The realist proportion size ensures trainees understand how to deal with such a delicate and small frame whilst delivering the potentially life-saving treatment.

Key features

  • Oral and nasal passages allow for realistic nose pinch required for mouth-to-nose
  • Natural obstruction of the airway allows students to learn the important technique of opening the airway
  • Capable of performing the head tilt/chin lift and jaw thrust manouver
  • Realistic chest movement means students can experience the proper technique required for chest compressions
  • Foreign-body airway obstruction feature allows the release of a foreign-body obstruction to be practised through back blows and chest-thrust techniques
  • Economical disposable airways
  • Removable and reusable faces

About the Manufacturer

Laerdal's beginnings date back to the 1940's where they started in a small publishing house, specializing in children's books and greetings cards.

Fast forward to the present day, Laerdal are one of the world's leading medical technology developers and their Resusci Anne range is used all over the world to teach CPR.

More Information

If you would like to learn more about the Baby Anne, the defibshop team are always here to help.

Call 800 989 7768 to speak to one of our friendly, expert advisors who 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.