Laerdal Baby Anne Dark

Laerdal Baby Anne Dark

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Laerdal Baby Anne Dark

Product Code 130-03050USA

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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 Dark will enable you to teach students how to effectively treat babies in a first aid emergency. Its life-size proportions provides insight as to how a responder would adapt first aid to fit and treat a small and delicate frame.

Ensuring your students are completely aware of the differences between CPR and infant CPR is essential to them being able to act with confidence in almost any emergency. The Baby Anne Dark will ensure that students can practice their life-saving skills on a manikin that emulates the size and stature of a baby so they're confident that if an emergency arose, they would be able to act.

Key Features

  • Realistic body features
  • Chest movement in the manikin to emulate real CPR on an infant
  • Oral and nasal passages to allow for mouth-to-mouth and nose pinch ventilation
  • Removable faces
  • Economical disposable airways
  • Head tilt, jaw thrust and chin lift allows learners to practice all CPR manouevers

About the Manufacturer

Laerdal's beginning dates back to 1940 where they started off as a small publishing house.

Fast forward to the present day, Laerdal are one of the market leading first aid developers and manufacturers. Their Little Anne training manikin is now being used all over the world to teach CPR.

More Information

If you would like more information about the Baby Anne Dark, the defibshop team are the ones with all the answers.

Call 888 820 0760 to speak to one of our product specialists and they'll be happy to share all their knowledge with you to help you find the perfect products for your needs and budget.

 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.