Laerdal Resusci Anne QCPR with carry bag
Laerdal Resusci Anne QCPR with carry bag
Product Code 171-00160USA
- Torso Manikin
- 3 Decorated Resusci Manikin Faces
- 2 Disposable Airways
- 2 Extra Compression Springs (Hard and Soft)
- Semi-Rigid Carry Bag with Integrated Kneel Mat
- 50 Resusci Manikin Wipes
- USB cable (for use with any USB power supply)
- User Guide
- Important Product Information
The Resusci Anne QCPR has been designed to help trainers provide an effective and realistic training experience for their learners and is also capable of providing real-time feedback about the CPR being delivered so students can quickly sharpen their skills.
The Resusci Anne QCPR manikin and the compatible feedback devices have been designed with simplicity and ease of use in mind and require minimal setup time, helping both trainers and trainees alike to focus on practising effective, high-quality CPR.
- Anatomically correct
- Compliant with the AHA guidelines for CPR and ECC
- Oral and nasal passages to allow for mouth-to-mouth and nose pinch practice
- Various chest springs enable different chest resistance for CPR practice
About the Manufacturer
Since 1960, Laerdal's Resusci Anne has been the preferred CPR training manikin of healthcare professionals and it has helped to train and educate over 400 million people.
Did you know, Laerdal's beginnings weren't in the medical industry, but in a small publishing house that specialized in children's books and greetings cards?
If you would like to learn more about the Resusci Anne QCPR with carry bag, speak to the defibshop team.
To speak to one of our advisors, call 800 989 7768 and they'll be happy to share their expertise 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.