Laerdal Little Family Pack
Laerdal Little Family Pack
Product Code 126-01050USA
- 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 provides trainers and learners alike with an entire age range of training manikins, allowing you to practice the different forms of CPR on their respective aged manikin.
Designed to display the anatomical differences between the different ages, the Little Family Pack will ensure you can provide CPR training for all ages so your learners feel confident in almost any cardiac emergency and understand what is required by each victim.
- 3 separate manikins
- Individual training mats for each manikin
- Economical disposable airways
- Additional manikin faces for replacement
About the Manufacturer
Laerdal's origins date back to the 1940's as a small publishing house, but they soon found their success after developing first aid manikins
Nowadays, Laerdal are one of the world's most renowned medical technology developers who solely devote their time to developing a varitey of products that are designed to asssit with emergency medicine.
If you would like to learn more about the Little Family Pack, the defibshop team are here to help.
Call 888 820 0760 and one of our Product Specialists will be happy to 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.