ZOLL AED Plus/Pro Stat-Padz II - single


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ZOLL AED Plus/Pro Stat-Padz II - single

Product Code 8900-0801-01usa

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In Stock

What's Included?

  • 1 pair of Stat-Padz II

With pre-connective ability, the Stat-Padz II for ZOLL AEDs allows users to deliver a quick response time, providing defibrillation if needed as soon as possible.

Electrodes are a vital component of your life-saving equipment as they provide the connection between AED and the casualty’s heart. As all electrodes are single use only, we advise on keeping a spare pair with your unit so you’re always able to deliver an effective rescue should your original set of electrodes become compromised.

Pad Features

  • Diagrams instructing where to place the pads
  • Pre-connected electrodes
  • Compatible with AED Plus and AED Pro
  • Improved gel formula increases conductivity
  • We advise that the pads should be replaced every 2 years

How to Use

Remove the electrode pads from their protective packaging and, following the instructions on the packet – apply them to the victim’s chest.

Once accurately placed, your AED will immediately begin to analyze the casualty’s chest and will advise whether a shock is required. Your AED will also instruct when to begin CPR, giving you confidence in the treatment you provide, whether this is your first or fiftieth rescue!

More Information

Do you have a question for our team regarding one of our products? No problem! Simply give our friendly team of advisors a call on 800 989 7768 and have all of your queries answered.

 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.