Laerdal Little Anne AED
Laerdal Little Anne AED
Product Code 122-01050USA
- Little Anne AED Manikin
- Soft Pack/Training Mat
- 2 Manikin Faces
- 2 Airways
- 6 manikin wipes
- User Guide
The Little Anne AED training manikin has been designed to create the most realistic training experience for your learners. Students can practice both their CPR skills on this manikin as well as AED implementation to help them gain an understanding of how to provide the most effective care for a victim of sudden cardiac arrest.
Designed to be durable and ready for heavy-duty use, the Little Anne AED training manikin allows for a hands-on training experience for all learners.
This specific manikin has recently been enhanced to provide learners with a more realistic training experience for both CPR and AED use, so your students will feel confident with the knowledge that they can assist a victim of cardiac arrest.
- Realistic airway that will only function if the learner performs an accurate head tilt, chin lift or jaw thrust
- Anatomically correct to help with AED pad placement and CPR hand placement
- Realistic oral and nasal passages
- Compatible with Laerdal's CPRmeter
- Optional clicker feature alerts the user to when they have achieved the correct compression depth
- Disposable airways
- Removable and reusable faces
About the Manufacturer
Starting off as a small publishing house that specialized in greetings cards and children's toys, after the death of a child during the turn of the 19th Century Åsmund S. Lærdal adopted the child's face for the mask of his newly developed resuscitation-training manikin.
He believed if a manikin was life-sized and life-like, learners would be better motivated and assisted to learn the life-saving steps.
If you require more information about the Little Anne AED, the defibshop team are always here to help.
Call 800 989 7768 to speak to one of our advisors who will be happy to 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.