Laerdal Little Family Pack Brown
Laerdal Little Family Pack Brown
Product Code 126-03050USA
- Large Family Pack Bag on Wheels
- Little Anne manikin:1 Training Mat, 2 Manikin Faces, 2 Little Anne Airways, 6 Manikin Wipes and User Guide
- Little Junior manikin: 1 Training Mat, 2 Manikin Faces, 2 Airways, 6 Manikin Wipes and User Guide
- Baby Anne manikin: 6 Airways, 10 Foreign Body Practice Objects and User Guide
The Little Family Pack Brown provides you with three separate manikins that will enable you to train your students on all types of CPR with the corresponding aged manikin.
With the Little Family Pack, you are provided with three differently aged manikins as this will allow you to teach the variances of CPR, depending upon the age of the victim. This will ensure that your students understand what is required of them, regardless of the age of the victim.
- Three separate manikins
- Oral and nasal passages
- Anatomically correct
- Head tilt and jaw thrust manouever
About the Manufacturer
Laerdal's beginning's date back to 1940 where they started in a small publishing office, specializing in greetings cards and children's books. As they started to develop first aid manikins, they started to see success.
Nowadays, Laerdal are one of the world's most well-known medical technology developers as they are continually developing products that assist in medical emergencies. These products range in CPR training, AEDs, airway management, patient simulation and more.
If you would like to learn more about the Lilttle Family Pack Brown, the defibshop team are here to help.
Call 888 820 0760 to speak to one of our experts and they'll happily assist you in any way they can.
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.