HeartSine Gateway


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HeartSine Gateway

Product Code ACC-GTW-US-01

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What's Included?

  • HeartSine Gateway
  • Carry Case
The HeartSine Gateway allows AED program managers to monitor a fleet of HeartSine AEDs across multiple locations.

Gateway will alert you of anything that needs attention such as reminders and expirations. Gateway communicates with LIFELINKcentral AED Program Management system or LIFENET System via WiFi and sends the results of the regular AED self-tests to these management systems.

Key Features

  • Wireless connectivity
  • Self-monitoring
  • Backward compatible
  • Low cost of ownership

(Dimensions: 6.69 in x 2.75 in x 1.97 in)

Compatible with all HeartSine Samaritan PAD models manufactured during or after 2013 (with a serial number beginning with “13” or above).

Connected Technology

HeartSine's Gateway allows AED owners to manage their HeartSine Samaritan PAD AEDs remotely by converting the device into a connected AED. By simply attaching Gateway to the top of the AED will connect the device and allow it to be remotely monitored.

LIFELINKcentral Program Manager: Once Gateway has successfully connected to LIFELINKcentral, this AED Program Management system will track the readiness of your AED, the Pad-Pak expirations, self-test results and more, to give you the peace of mind that your AED is always ready to be used in a rescue.

Readiness is made easy with Gateway as it independently monitors, sending email alerts when necessary to inform the owner of any issues such as a low battery or change in temperature. 

More Information

If you have any questions regarding the HeartSine Gateway or any of our other products, do not hesitate to get in touch with a member of the team by calling 800 989 7768. 

 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.