Physio Control QUIK-COMBO 3-lead Patient Simulator


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  • quik-combo-3-lead-patient-simulator

Physio Control QUIK-COMBO 3-lead Patient Simulator

Product Code 11996-000310

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What's Included?

  • QUIK-COMBO 3-lead Patient Simulator

The QUIK-COMBO 3-lead Patient Simulator from Physio-Control connects directly to the Lifepak AED to enable trainers to provide an insightful and interactive training experience for their students.

After connecting the QUIK-COMBO 3-lead Patient Simulator to the Lifepak AED, it is capable of simulating 17 ECG rhythms, including various fibrillations, tachycardias and bradycardias.

Having the capability of providing an insight to a variety of fibrillations will provide your students with the most effective training and will equip your them with the knowledge and confidence of how to act during these emergencies.

About the Manufacturer

Physio Control are a world leader in the development and manufacturing of AEDs that can be used by both medical professionals and first-time responders.

They take their responsibilities very seriously and continually develop life-saving technologies for a variety of domains.

More Information

If you require more information about the QUIK-COMBO 3-lead Patient Simulator, get in touch with the team here at defibshop.

Call 800 989 7768 and one of our friendly advisors will be happy to share their knowledge with you.

 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.