Little Anne QCPR 4-Pack Dark Skin


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Little Anne QCPR 4-Pack Dark Skin

Product Code 124-03050USA

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What's Included?

  • 4 Little Anne QCPR Dark Skin Manikins

Thanks to the recent update, the Little Anne QCPR is capable of providing your learners with feedback on the CPR they're practising, helping to boost their confidence in their CPR delivery.

This four-pack option is a great choice for trainers who train larger groups and require more than one manikin for their courses.

Capable of providing real-time feedback to learners, the QCPR manikins will ensure your trainers understand how to deliver effective CPR, with confidence.

Key Features

  • Durable
  • Anatomically correct
  • Provides feedback to learners about their CPR
  • Lightweight
  • Portable

About the Manfacturer

Originally starting out as a small publishing house that specialized in children's books and greetings cards, Laerdal went onto develop children's toys which eventually led them to develop first aid manikins.

Fast forward to the present day and Laerdal is one of the world's most recognized developers of life-saving technology, boasting innovations in CPR training, airway management, AEDs and patient simulation.

More Information

If you would like to learn more about the Little Anne QCPR 4-Pack Dark Skin, the defibshop team are always here to help.

To speak to one of our advisors, call 800 989 7768 and one of our team members will be happy answer your questions and queries.

 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.