Laerdal Resusci Anne QCPR AED with Carry Bag

Laerdal Resusci Anne QCPR AED with Carry Bag

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Laerdal Resusci Anne QCPR AED with Carry Bag

Product Code 173-00150USA

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What's Included?

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

Realistic and designed for minimal setup time, the Resusci Anne QCPR helps almost any user to focus on learning and improving their CPR skills.

The Resusci Anne QCPR is capable of providing real-time feedback to learners, allowing them to quickly improve their CPR skills, so should an emergency arise they will feel confident enough to intervene and provide the required treatment.

Key Features

  • Realistic
  • Durable
  • Anatomically correct
  • AHA Guidelines for CPR and ECC compliant
  • Appropriate chest resistance
  • Head tilt, jaw thrust and chin lift manoeuvers

About the Manufacturer

Laerdal are one of the world's leading medical equipment manufacturers as they continually develop products that assist with CPR training, airway management, patient simulation and defibrillation.

Since 1960, the Resusci Anne has been the preferred CPR training manikin of professionals and has helped to train mroe than 400 million people in life-skills.

More Information

If you require more information about the Resusci Anne QCPR AED with carry bag, the defibshop team are always here to help.

Call 888 820 0760 to speak to one of our experts and they'll be happy to 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.