ZOLL Stat-Padz II Bundle (Pack of 2)
ZOLL Stat-Padz II Bundle (Pack of 2)
Product Code 8900-0802-01bUSA
- Two sets of Stat-Padz II Electrode Pads
With pre-connective ability, the Zoll Stat-Padz allow you to prepare for a rescue ahead of time to ensure you’re able to deliver life-saving care as soon as possible in the event of a cardiac arrest.
As one of the core components to a successful rescue and a single-use only product, we recommend this bundle pack of two so you can keep a spare pair of electrode pads with your AED at all times.
- 2 sets of pads
- Pre-connected electrodes
- Clear diagrams showing where to lay the pads
- We advise that the pads should be replaced every 2 years
How to Use
Remove the electrodes from their packaging and apply them to the victim’s chest, following the diagrams on the pack as a guide. Once the pads have been attached, your AED will automatically begin analyzing the patient’s heart rhythm to locate a shockable rhythm. If a shockable rhythm is found, your AED will advise shock delivery followed by CPR which you’ll be guided through step by step.
Never used an AED before? Not to worry, all ZOLL AEDs are equipped with both visual and vocal prompts so you’ll be assisted every step of the way to deliver the most effective care possible.
Want to discuss the Stat-Padz II bundle before you purchase? No problem, the helpful defibshop team are on hand to help. You can call 800 989 7768 where one of our knowledgeable advisors will answer any queries you may have.
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.