Laerdal Resusci Anne QCPR AED with trolley suitcase

Resusci-Anne-QCPR-AED-with-trolley-suitcase

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Laerdal Resusci Anne QCPR AED with trolley suitcase

Product Code 173-01260USA

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What's Included?

  • Full-body Manikin
  • 3 Decorated Resusci Manikin Faces
  • 2 Disposable Airways
  • 2 Extra Compression Springs (Hard and Soft)
  • Laerdal LINK Training Pads
  • Kneel Mat
  • Jacket, Pants
  • 50 Resusci Manikin Wipes
  • USB Cable (for use with any USB power supply)
  • User Guide
  • Important Product Information

Designed to effectively facilitate training for individuals and high-performance groups, the Resusci Anne QCPR AED will ensure that your students are confident in dealing with a cardiac emergency.

Designed to provide the most realistic training experience possible for your students, the Resusci Anne QCPR AED allows you to provide real-time feedback on the quality of the CPR being delivered, as well as train them in using an AED.

Key Features

  • Realistic
  • Durable
  • Anatomically correct
  • Compliant with AHA Guidelines for CPR and ECC
  • Appropriate chest resistance
  • Head tilt and chin lift manouevers

About the Manufacturer

Laerdal are one of the world's leading medical equipment manufacturers, dedicated to developing products and technology that can assist in CPR training, airway management, defibrillation and patient simulation.

Did you know, Laerdal started off in a small publishing house that specialized in children's books and greetings cards?

More Information

If you require more information about the Resusci Anne QCPR AED with trolley suitcase, get in touch with the defibshop team.

Simply call 800 989 7768 to speak to one of our friendly experts who will happily help you find the perfect products for your needs and budget.

 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.