Philips HeartStart Event Review Software Site-wide License

Philips HeartStart Event Review Software Site-wide License

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Philips HeartStart Event Review Software Site-wide License

Product Code 861489USA

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What's Included?

  • HeartStart Event Review Software Site-wide License

HeartStart Event Review Software provides the user with easy-to-use data management applications for electronically managing the data that has been collected during the HeartStart AED's usage.

Whether you're interested in data collection, case review, response analysis, trending data or performance evaluation, the HeartStart Event Review Software enables the user to view all of these data types.

The software accepts and presents ECG case data, including shock and audio (if recorded) from Philips, Laerdal, Hewlett-Packard and Agilent AEDs. The software also allows you to round out the data with the case detail by adding notes and completing data entry screens.

Key Features

  • Reporting functionality
  • Integrate ECGs from multiple AEDs into one case for a complete event history
  • Information sharing
  • Email cases to others who are running the software so they can view them
  • Easy-to-use
  • On-screen assistance
  • Can be used to reconfigure AED to 'hands-only' CPR protocol

About the Manufacturer

Philips are one of the most recognisable manufacturers in the AED industry. Their user friendly AED range caters for both trained and untrained responders, allowing rescuers of all training levels to act during an emergency with confidence.

More Information

If you would like to learn more about the HeartStart Event Review Software Site-wide License, the team here at defibshop are on hand to help.

Get in touch by calling 888 820 0760 and one of our friendly experts will happily assist 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.