Laerdal Resusci Anne QCPR AW
Laerdal Resusci Anne QCPR AW
Product Code 172-01250USA
- Full-body Manikin
- 2 Extra Compression Springs (Hard and Soft)
- Airway Lubricant
- Eye Set
- 50 Resusci Manikin Wipes
- Kneel Mat
- USB Cable (for use with any USB power supply)
- User Guide
- Important Product Information
The Resusci Anne QCPR manikin is capable of providing your learners with real-time feedback about the CPR they're delivering, so they can quickly improve their skills and boost their confidence in the skill.
Requiring minimal setup time and designed to be easy to use the Resusci Anne QCPR training manikin helps your learners to focus on learning and providing high-quality CPR to a patient in need.
- Anatomically correct
- Compliant with AHA Guidelines for CPR and ECC
- Appropriate chest resistance
- Head tilt, chin lift and and jaw thrust manouevers
About the Manufacturer
Laerdal's beginnings are quite different to any other medical equipment manufacturers. Did you know that they started in a small publishing house that specialized in greetings cards and children's books?
Since then, Laerdal have become one of the world's most recognised medical equipment manufacturers, developing products that cater for CPR training, airway management, defibrillation and patient simulation.
If you would like to learn more about the Resusci Anne QCPR AW, speak to the defibshop team.
To speak to one of our friendly experts, simply call 800 989 7768 and they'll 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.