Laerdal Little Anne 4-Pack
Laerdal Little Anne 4-Pack
Product Code 121-01050USA
- 4 Little Anne Training Manikins
- 4 Individual soft pack/ training mats
- 1 large 4 pack carry case
- 8 manikin faces
- 8 airways
- Manikin wipes
Designed to provide the most realistic training experience possible for first aid learners, the Little Anne training manikin will ensure your learners understand what is required of them in an emergency, allowing them to act with confidence.
If you're a first aid trainer and want to provide the most effective and realistic training experience for your learners, the Little Anne 4-Pack is a great option as multiple learners can use the manikin to practice their CPR skills and increase their confidence.
- Realistic airway construction
- Head tilt feature
- Anatomically correct
- Compatible with Laerdal's CPRmeter to enhance the training experience and receive real-time feedback
- Ergonomic disposable airways for quick and easy clean-up after the session
- Removable and reusable faces
- Optional clicker feature which helps to achieve the correct chest compression depth
- Lightweight design
About the Manufacturer
Unlike other medical technology manufacturers, Laerdal's beginnings were in a completely different field. Originally, Laerdal started off in a small publishing house, specializing in greetings cards and children's books. This led them to develop children's toys and eventually, first aid manikins.
After decades of development, Laerdal are on the of the leading medical technology developers in the world, dedicating their time to CPR training products, airway management, AEDs and patient simulation.
If you would like to learn more about the Little Anne 4-Pack, the defibshop team are here to help.
Call 888 820 0760 to speak to one of our advisors.
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.