Resusci Anne Wireless SR software (3 licenses)

Resusci Anne Wireless SR software (3 licenses)

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Resusci Anne Wireless SR software (3 licenses)

Product Code 202-56050

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What's Included?

  • Three Liscense Keys for SkillReporter (PC Software)

SkillReporter provides trainers with the flexibility to provide Quality CPR Training in almost any location. In this package, you will receive 3 software licenses.

This easy-to-use software comes with Multi-Manikin Overview options and real-time CPR performance feedback which will help trainers to educate their students in their actual working environments.

Operating system requirements: Windows XP, Windows Vista, Windows 7 and Windows 8 (excludes Windows 8 RT light version).

Key Features

  • Easy to use
  • Measures the quality of the CPR being delivered, providing real-time feedback
  • Multi-Manikin overview options (up to six manikins)
  • Compatible with the Resusci Anne QCPR and Resusci Baby QCPR manikins

About the Manufacturer

Laerdal started off in 1940 as a small publishing hosue that specialized in children's books and greetings cards.

Fast forward to the present day, Laerdal are one of the world's leading medical equipment manufactureres.

Their Resusci Anne training manikins have helped to educate over 400 million people in life-skills and is the chosen manikin of many medical professionals.

More Information

Think this might be the product for you? If you have any additional questions, don't hesitate to ask!

To speak to one of our advisors, call 888 820 0760 and they'll be happy to help answer any questions or queries you may have.

 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.