Laerdal Little Anne QCPR 4-Pack
Laerdal Little Anne QCPR 4-Pack
Product Code 124-01050USA
- 4 Little Anne QCPR Manikins
The Little Anne training manikin has been designed with convenience and durability, to allow for extensive use during training lessons. Anatomically correct, this manikin will allow you to provide the most realistic training experience for your learners.
The four-pack option is a great choice for trainers who train larger groups and require more than one manikin for learners to practice their CPR skills on.
After receiving a recent update, the Little Anne QCPR is capable of providing learners with feedback on the CPR they're delivering, enhancing their skills and boosting their confidence.
- Anatomically correct
- Provides feedback to learners about their CPR delivery
About the Manufacturer
Unlike other competitors who's history traces back to the medical field, Laerdal orginated from a small publishing house that specialized in children's books and greetings cards. This led them to develop children's toys and eventually first aid manikins.
Since then, Laerdal have become one of the world's most well known medical technology developers, dedicating their time to developing new, life-saving equipment ranging from patient simulation to AEDs and CPR training to airway management.
If you require more information, the defibshop team are here to help.
To speak to one of our friendly experts, call 800 989 7768 and they'll be happy to help you in anyway they can.
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.