ZOLL AED Plus Trainer II
ZOLL AED Plus Trainer II
Product Code 8008-0050-01
- ZOLL AED Plus Trainer
- Wireless Remote Controller
- 1 set of CPR-D training electrodes
- 1 set of replacement gels
- 4 D-Cell batteries
- 2 AA batteries
- Operators Guide
- Six-month limited warranty.
With the ability to provide the same functions and features as if it were a clinical unit, the ZOLL AED Plus Trainer II will provide your students with an effective training experience complete with electrode pad placement, CPR and ‘shock’ delivery.
A training unit provides potential users with the vital hands-on experience of using an AED, in a relaxed and comfortable setting. As cardiac emergencies can be incredibly stressful scenarios, it’s important rescuers learn the vital steps to take beforehand, to ensure they’re equipped with the knowledge to act, should an emergency take place.
How to Use
This particular training unit will allow learners to get to grips with the unique characteristics of your AED, including understanding the voice and vocal prompts as they deliver a rescue, step by step on a manikin. This training method helps to boost confidence and will improve accuracy in electrode pads placement and how to deliver effective CPR.
This training unit provides real-time CPR feedback and will instruct users when to deliver compressions as well as whether they need to ‘push harder’ or whether ‘good compressions’ are being applied. CPR is a vital part of a cardiac rescue process, so giving your students the opportunity to learn this skill beforehand is incredibly important.
Considering the ZOLL AED Fully Auto Trainer II? If you have any questions, please don not hesitate to get in touch with the defibshop team.
With over a decade of experience in the AED business, you can be sure that the advice we provide is knowledgeable, correct and tailored to fit your needs; call us direct 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.