Laerdal Resusci Anne First Aid with carry bag
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Laerdal Resusci Anne First Aid with carry bag
Product Code 170-00150
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What's Included?
- Torso Manikin
- 3 Decorated Resusci Manikin Faces
- 2 Disposable Airways
- Semi-rigid Carry Bag with integrated kneel mat
- Jacket
- 50 Resusci Manikin Wipes
- User Guide
- Important Product Information
This specific configuration of the Resusci Anne First Aid is just the torso of the manikin which allows your students to quickly sharpen their CPR skills on a high quality, realistic manikin.
The Resusci Anne First Aid offers trainees optimal realism and the chance to quickly sharpen their CPR skills.
The physiologically correct design of the torso allows students to identify anatomical landmarks on the manikin which reflects where they would be on a patient.
Key Features
- Natural obstruction of the airway allows students to practice opening the airway
- Head tilt, chin lift and jaw thrust manoeuver
- Carotid pulse simulation to enable students to practice checking for a pulse
- Removable and reusable faces
- Disposable non-rebreathing airways
About the Manufacturer
After decades of development, Laerdal are one of the world's leading first aid manufacturers whose training manikins are used all over the world to help educate people about CPR.
Did you know they started off as a small publishing house back in 1940 that specialized in greetings cards and children's books?
More Information
If you require more information about the Resusci Anne First Aid with carry bag, speak to the defibshop team.
Call 800 989 7768 and one of our friendly experts will be happy to share their knowledge with you.
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.