HeartSine Samaritan PAD 360P Trainer With Remote


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  • heartsine-sam-360p-aed-trainer

HeartSine Samaritan PAD 360P Trainer With Remote

Product Code 11516‐000091USA

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What's Included?

  • Samaritan PAD 360P Trainer With Remote

The training unit of the Samaritan PAD 360P from Heartsine displays to trainees exactly how a clinical unit would act if activated during a cardiac emergency.

One of the main benefits of a training unit is that it helps students become familiar with the specific features and functions of this AED.

By training your students on a specific training unit, they will be completely aware as to how the clinical counterpart will react once activated in a real-life emergency. Having this knowledge will ensure that your students can react fast and with confidence.

The additional feature of the remote allows trainers to bypass any of the rescue stages, if needed and prompt a simulated shock from the AED.

About the Manufacturer

Heartsine have continually dedicated their time to developing and innovating affordable life-saving technologies. Their devices are simple and user-friendly, so regardless of the responder's training level, they will be able to respond and use the AED confidently.

More Information

If you require more information about the Samaritan PAD 360P Trainer With Remote from Heartsine, the team here at defibshop are on hand to help.

To speak to one of our expert advisors, call 800 989 7768 and one of our experts will be happy to help.

 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.