Laerdal Mini Anne Plus (10) Lt


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  • mini-anne-plus

Laerdal Mini Anne Plus (10) Lt

Product Code 106-00150USA

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What's Included?

  • 10 manikins (light skin)
  • 10 kneel mats
  • 10 pump bags
  • 1 carry bag
  • 2 mesh collection bags
  • 10 face masks
  • 50 manikin wipes
  • 50 airways

Designed to increase your student's efficiency whilst maintaining effective CPR, the Mini Anne Plus 10 pack will ensure you have everything you need to provide effective training for your learners.

Designed to be simple, but effective the Mini Anne Plus is a cost-effective solution for all trainers looking to teach CPR in classes both small and large.

Key Features

  • 10 individual manikins to allow for increased students hands-on time
  • Pump bag design allows for a simple, hygenic inflation of the manikin
  • All kept in one convenient bag

About the Manufacturer

Starting off as a small publishing house in 1940 that specialized in greetings cards and children's books, Laerdal have gone on to become a market leader in first aid equipment.

Inspired by a girl who was pulled from the River Seine in Paris, Asmund Laerdal adopted her face for the very first Resusci Anne manikin as he believed that if the manikin was life-size and life-like, learners would be better motivated to practice their life-saving skills.

More Information

If you would like to learn more about the Mini Anne Plus (10) Lt, the defibshop team are here to answer all your questions.

Call 888 820 0760 and one of our advisors will 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.