Heartsine Samaritan Pedi-Pak Pediatric Cartridge

Heartsine Samaritan Pedi-Pak Pediatric Cartridge

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Heartsine Samaritan Pedi-Pak Pediatric Cartridge

Product Code 11516-000004

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What's Included?

  • Samaritan Pedi-Pak Pediatric Cartridge

Designed for use with the Samaritan PAD AED range from Heartsine, the pediatric PADs will deliver a lower level shock that is safe for the heart of a child.

With the ability to lower the joule output, you can have peace of mind that your Heartsine Samaritan PAD can deliver the potentially life-saving treatment to a pediatric victim of sudden cardiac arrest.

With a connected battery and Pad-Pak, you only have one expiry date to remember so replacing your accessories couldn't be easier!

Key Features

  • Single use pediatric cartridge
  • Battery life for up to 60 shocks or 6 hours of continuous operation
  • Audible prompt when the battery power is down to 10 shocks or less
  • Reduces the joule output to a safer level that is safer and suitable to use on a child

How to Use

If a child has fallen victim to sudden cardiac arrest, it is essential that the life-saving treatment is delivered as swiftly as possible as this provides the casualty with the highest chance of survival.

When applying the pads to the victim, the pads should be placed in accordance to the diagrams on the reverse of the pads. It is important that these are followed as pad placement on a child is different than and adult.

Once the pads have been successfully applied, they will analyse the heart rhythm and relay in the information back to the AED which will then make a decision whether the patient requires a shock or not. If no shock is required, no shock will be delivered.

More Information

If you require more information about the Samaritan Pedi-Pak Pediatric Cartridge from Heartsine, the defibshop team are here to help.

To speak to one of our advisors, call 800 989 7768 and one of our friendly experts will happily share their knowledge with 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.