Little Anne QCPR
Little Anne QCPR
Product Code 123-01050ie
- Little Anne QCPR Manikin
- 2 manikin faces
- 2 airways
- 6 manikin wipes
- Jacket for manikin
- Soft pack carrying case/training mat
Designed for heavy duty use, the Little Anne QCPR training manikin will ensure your students feel confident in the CPR they're delivering by providing feedback so their skills can continually be developed.
Due to the recent update that the Little Anne manikin has been provided with, the Little Anne QCPR manikin is capable of providing feedback to your learners about the CPR they're delivering. This feedback has been designed to help them deliver effective CPR to the manikin, whilst also feeling confident enough to deliver the skill to a casualty.
- Anatomically correct
- Feedback provided to improve CPR skills
About the Manufacturer
Laerdal's history is very different to other medical manufacturers; they started off as a small publishing house that specialised in children's books and greetings cards. Since then, they went on to develop children's toys which eventually led to them developing first aid manikins.
Fast forward to the present day, Laerdal is one of the world's leading medical technology manufacturers that caters in CPR training, airway management, defibrillators and patient simulation.
If you would like to learn more about the Little Anne QCPR, the defibshop team are here to help.
Want to know why you should choose us? Press play and find out more...
Buying a defibrillator? You’ve come to the right place...
- With nearly 20 different defibrillator models available, our defibshop team knows them all and can help you decide which device suits your budget, environment and business
- We have over 20 staff on hand who can offer friendly and impartial advice on all things defibrillators
- Not only do we provide a free battery and electrode pad reminder service, but we will replace your electrode pads for free if they are used within two years of purchase
Did you know that we're an Award Winning company?
We’re not a company for bragging but we like to think that our trophy cabinet indicates that you have come to a trustworthy and dependable company who recognises you are making a significant and fantastic step when buying a defibrillator.
We were recently listed in the Small Business category of the 'Great Place to Work: Best Workplaces 2014’ whilst we have also won accolades in the Salford Business Awards 2014 & 2012, Investors in People Bronze award and an Insight 100 Customer Service Award in Training Services 2013.
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.