HeartSine Samaritan PAD 350P Trainer With Remote


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  • Samaritan-PAD-350P-Trainer-With-Remote

HeartSine Samaritan PAD 350P Trainer With Remote

Product Code 11516-000059

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What's Included?

  • Samaritan PAD 350P Trainer
  • Remote
The HeartSine Samaritan PAD 350P Trainer With Remote allows the trainer to become familiar with how they would use a live unit in an emergency situation.

The training unit for the Samaritan PAD 350P will allow trainees to familiarize themselves with the features of the AED, becoming confident in using the unit in preparation for responding to a real-life emergency.

How to Use

Trainers can use the remote control to simulate the whole process of defibrillation from applying the pads, to delivering the life-saving shock.

Each unit includes training pads, rechargeable battery, battery charger, and user manual. There are 8 different rescue scenarios and trainers can build confidence during a mock rescue.

This training unit ensures the learner is able to act confidently and effectively in providing life-saving treatment if a real-life emergency were to arise.

About the Manufacturer

Since their establishment in 1998, HeartSine have developed technologies that are easy-to-use to provide life-saving treatment for SCA victims. 

More Information

You can contact us for more information about the Samaritan Pad 350P trainer or another product from our range. Our defibshop team are also happy to help with any enquiries that you have. Give them a call on 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.