Laerdal Little Anne Brown
Laerdal Little Anne Brown
Product Code 120-03050
- Little Anne Manikin with Brown Skin
- Soft Pack/Training Mat
- 2 Manikin Faces
- 2 Airways
- 6 manikin wipes
- User Guide
The Little Anne Brown training manikin will assist trainers in providing the most realistic first aid training. Designed for hands-on use, your students will be confident that they can act during a cardiac emergency and understand what is required of them and why.
Strong, sturdy and anatomically correct, the Little Anne Brown will ensure that your learners get the most out of their training experience so they can confidently act in a real-life emergency.
- Portable and lightweight
- Optional clicker to assist with achieving the correct chest compression depth
- Realistic oral and nasal passages to allow for mouth-to-mouth ventillation
- Compatible with Laerdal's CPRmeter to further enhance training and receive real-time feedback
- Removable and reusable faces
- Realistic airway construction
About the Manufacturer
Unlike other manufacturers who's history is medical technology and AEDs, Laerdal's is something quite different as they started off as a small publishing house that specialized in greetings cards and children's books. This led them to start developing children's toys and eventually, first aid manikins.
Nowadays, Laerdal is one of the world's leading medical technology developer as they dedicate their time to developing a variety of products that filter under the medical field ranging from CPR training to airway management and AEDs to patient simulation.
If you require more information about the Little Anne Brown, speak to one of our experts here at defibshop.
To speak to one of our team members, call 800 989 7768 and they'll be happy to answer 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.