Physio Control LIFEPAK CR2 Trainer
Physio Control LIFEPAK CR2 Trainer
Product Code 11250-000163ie
- Lifepak CR2 Trainer
- Lifepak CR2 training electrodes
The Lifepak CR2 training unit has been designed to fully simulate the functions and features of a clinical Lifepak CR2 in order to provide learners with a realistic experience.
Learners will become familiar with how the device reacts in a real life cardiac emergency by going through each stage of the rescue process, so if the clinical device was required in a real life emergency, they would know exactly what to expect from the defibrillator and what prompts it will provide them with to assist with the rescue, putting them at ease and preparing them for this real life scenario.
How to Use
The Lifepak CR2 Trainer can be configured to different training scenarios from the panel underneath the electrode tray.
Trainers can simulate both a fully-automatic and semi-automatic Lifepak CR2, to gain an understanding of the differences between the two different configurations and what is required by each clinical device in an emergency.
This training experience will ensure that they are ready to act, should a real-life cardiac emergency arise. Learner's confidence will grow as they familiarise themselves with all the different features of the Lifepak CR2 as they will know exactly how this unit will respond if required in a cardiac emergency.
About the Manufacturer
Physio Control have become one of the world's most recognised and well-known defibrillator manufacturers. All devices designed and manufactured by Physio-Control have been designed to cater for all levels of training so whether you're a medical professional or a first-time responder, you can deliver the potentially life-saving treatment to the patient, with confidence.
Want to know more? If you would like to learn more about the Lifepak CR2 Trainer, the defibshop team are here to help. To speak to one of our advisors call 015079907.
Want to know why you should choose us? Press play and find out more...
Buying a defibrillator? You’ve come to the right place...
- With nearly 20 different defibrillator models available, our defibshop team knows them all and can help you decide which device suits your budget, environment and business
- We have over 20 staff on hand who can offer friendly and impartial advice on all things defibrillators
- Not only do we provide a free battery and electrode pad reminder service, but we will replace your electrode pads for free if they are used within two years of purchase
Did you know that we're an Award Winning company?
We’re not a company for bragging but we like to think that our trophy cabinet indicates that you have come to a trustworthy and dependable company who recognises you are making a significant and fantastic step when buying a defibrillator.
We were recently listed in the Small Business category of the 'Great Place to Work: Best Workplaces 2014’ whilst we have also won accolades in the Salford Business Awards 2014 & 2012, Investors in People Bronze award and an Insight 100 Customer Service Award in Training Services 2013.
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.