Laerdal Little Anne QCPR Dark Skin

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Laerdal Little Anne QCPR Dark Skin

Product Code 123-03050USA

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What's Included?

  • Little Anne Training Manikin
  • 2 manikin faces
  • 2 airways
  • 6 manikin wipes
  • Jacket for manikin
  • Soft pack carrying case/training mat

Designed for excessive use, the Little Anne training manikin is now capable of providing your learners with feedback on their CPR skills, allowing them to continually improve.

The newly updated Little Anne training manikin is now capable of providing your learners with feedback on the CPR they're performing. This feedback will continually allow them to improve their CPR skills during the session and increase their engagement with the class.

Key Features

  • Portable
  • Lightweight
  • Anatomically correct
  • Feedback provided to improve CPR skills

About the Manufacturer

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

Laerdal are now one of the world's most well known medical technology developers. They continually dedicate their time to developing new life-saving equipment, ranging in CPR training, patient simulation, AEDs and more.

More Information

If you require more information about the Little Anne QCPR Dark Skin, speak to the defibshop team.

Call 800 989 7768 and one of our team members will be happy to share their knowledge with you.

 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.