Laerdal Mini Anne Plus (10) Dk


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Laerdal Mini Anne Plus (10) Dk

Product Code 106-00250USA

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What's Included?

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

Designed to provide a cost-effective solution for teaching CPR, the Mini Anne Plus (10) Dk will ensure you have everything you need to teach your students effective CPR.

Ensuring your learners are confident in the delivery of CPR, is essential. The Mini Anne pack of 10 will ensure that all your students have the opportunity to practice and improve their CPR skills on one of the manikins.

Key Features

  • 10 individual manikins allowing for more hands-on time
  • New pump bag design provides a simple and hygienic inflation method
  • All kept in one convenient bag
  • About the Manufacturer

    Starting off in 1940 as a small publishing house that specialized in children's books and greetings cards, Laerdal have gone on to become one of the world's leading first aid equipment manufacturers.

    Catering in a variety of fields, Laerdal continually dedicate their time to developing products that can assist in fields such as CPR training, airway management, AEDs and patient simulation.

    More Information

    If you require more information about the Mini Anne Plus (10) Dk or any other product listed on our website, the defibshop team are here to help.

    Call 800 989 7768 to speak to one of our friendly experts and they'll happily assist 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.