Physio Control TrueCPR
Physio Control TrueCPR
Product Code 80596-000003USA
- TrueCPR device
Effective CPR plays a vital role when rescuing a victim of cardiac arrest. It is the first link in the chain of survival and crucial in the process of saving a life.
The True CPR coaching device by Physio Control measures the quality of the CPR being delivered to the victim. The compression depth, rhythm, and movement are monitored by the device to help the rescuer to maintain consistency by providing quality feedback.
- Monitors the rescuer's technique to enhance treatment
- Effective feedback is delivered to provided to help improve early treatment
- Visual monitor aids are right in the eye line of the rescuer to help maintain CPR assessment during and after treatment.
- Accurate depth measurement is assisted through tracking a magnetic field between the patient’s chest and back
This small, but effective device helps to provide the best CPR feedback possible to enhance treatment, increasing chances of survival for the victim.
True CPR has a target compression depth range of 5 to 6 centimeters and has a metronome feature to help keep rescuers on a steady CPR rhythm. This dinky device boasts an impressive IP rating of 55, meaning it is highly resilient to water and dust and it can even store three 60-minute compression session data, or up to six sessions totaling 180 minutes.
When all available data has been used on the device, the data from the oldest session is automatically overwritten. This can then be transferred to a computer by USB connection.
Got an unanswered question about the TrueCPR product? No matter what your question or query, the defibshop team are here to help.
Get in touch with our team by calling 800 989 7768 and one of our friendly, impartial advisors will assist you with your questions.
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.