Baby Anne Dark 4-Pack


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  • baby-anne-dark

Baby Anne Dark 4-Pack

Product Code 131-03050

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En existencia

What's Included?

  • 4 Baby Anne Manikins
  • Soft Pack
  • 24 Airways
  • 40 Foreign Body Practice Objects
  • Directions for Use

The Baby Anne training manikin will help ensure that your students are aware of how to effectively treat a baby in a first aid emergency. The life-size proportions of the manikin will help trainees to understand how to effectively deliver CPR to such a small and delicate frame.

The Baby Anne training manikin will ensure your learners are completely aware of how to deliver effective CPR to a first aid emergency that involves a baby.

The four-pack option is perfect for trainers who teach larger groups of students. Providing more than one manikin to train on will ensure all your students can practice and improve their CPR skills during the class.

Key Features

  • Realistic features
  • Chest movements allow students to experience the correct CPR technique
  • Oral and nasal passages allow for nose pinch and mouth-to-mouth ventilation
  • Head tilt, jaw thrust and chin lift manouevers
  • Economical disposable airways
  • Removable and reusable faces

About the Manufacturer

Unlike other manufacturers, Laerdal's beginnings were in a small publishing house that specialized in children's books and greetings cards. Soon after they went on to develop children's toys and eventually first aid manikins.

Laerdal are one of the market leaders in first aid training products, but also provide products that range in CPR training, airway management, AEDs and patient simulation.

More Information

If you would like to learn more about the Baby Anne Dark 4-pack, speak to the defibshop team.

Simply call 888 820 0760 to speak to one of our friendly experts and they'll assist you with any questions or queries 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.