Head Section Model


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  • Head-Section-Model

Head Section Model

Product Code 10900

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What's Included?

  • 1 Head Section model
We are the number 1 distributor for all first aid products. Gives precise example of how to manage the head and tilt in the correct way, when administering CPR, so that the airway is as clear as possible.

This head section model from Laerdal Medical is designed to help learners see how the head and neck works during the administering of cardiopulmonary resuscitation.

A simple design with movable components, the model will ensure trainees can see how CPR helps in an emergency situation and how parts of the head move during a rescue attempt.

Key features

  • Easy to operate head section model with moving tongue and throat
  • Gives precise examples of how to manage the head and tilt it in the correct way
  • Lightweight and easy to transport

About the Manufacturer

When the company moved into the production of first aid training equipment, in particular the design and manufacturer of the Resusci Anne training manikin, Laerdal Medical dedicated itself to advancing the cause of resuscitation and emergency care.

Their initial toy production line was de-emphasised, and consequently a new logo was needed to reflect their new mission. They chose the ancient symbol of the Good Samaritan, depicting the tale of a traveller whose selfless compassion and care saved the life of a total stranger.

More Information

If you would like to learn more about the head section model from Laerdal Medical, then our expert and friendly defibshop team are always on hand to help.

To get in touch, give us a call on 0845 071 0830.

 Want to know why you should choose us? Press play and find out more...

And if it couldn't get any better.. 

  • We have over 50 different defibrillators available and we can help you decide the best one for you
  • We have over 200 trainers nationwide to deliver nationally accredited training in the use of a defib and CPR
  • Over 20 staff on hand to offer impartial advice on all things defibrillators
  • 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

Did we also mention we are an Award Winning company?

We’re sure that you have been past our Home Page, but in case you haven’t, skipping the intro and getting stuck into the world of defibrillators, we are an award winning company.

In 2014 we added an impressive trophy to the cabinet by being listed 22nd in the ‘Great Place to Work: Best Workplaces 2014’ Small Business Category.

We also have to our name Salford Business Excellence Award Runner Up 2017, 2014 & 2012, Investors in People – Bronze Award and an Insight 100 Customer Service Award in Training Services 2013 award.

We also have a number of accreditations under our belt, including being a TQUK Diamond Approved Centre, ISO 9001 and 14001 and 27001. 

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.