Cardiac Science Powerheart G3 Pediatric Defibrillation Electrodes
Additional Images
Cardiac Science Powerheart G3 Pediatric Defibrillation Electrodes
Product Code 9730-002USA
0 reviews
In Stock
What's Included?
- 1 Set of Powerheart G3 Electrode Pads
Being prepared is the key to assisting in the event of an emergency. By keeping a set of Powerheart G3 Pediatric Pads with your rescue kit ensures you are always able to take action should a child fall victim to cardiac arrest.
If your AED is located somewhere that children are around, it is important to have the appropriate equipment that could save a child's life.
These pads will ensure the joule output is reduced, making it safe for young hearts.
Key Features
- Easy to open foil packaging keeps the electrode pads safe and secure
- Clear images on the pads to indicate where they should be placed on the patient
- Designed to be preconnected, saving time in an emergency
- Super sticky adhesive to ensure placed pads do not move
- Reduced joule output from the AED to ensure safe treatment for a child
When to use
Sadly, SCA does not discriminate meaning that children can also suffer a cardiac arrest. It is, therefore, crucial to have pediatric pads for safe and effective treatment for a child that has suffered a cardiac arrest.
More Information
If you have any questions regarding the Cardiac Science Powerheart G3 Pediatric Defibrillation Electrodes, do not hesitate to get in touch. A member of the team will be more than happy to help. Just call 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.