Laerdal Little Jr. Brown Skin
Laerdal Little Jr. Brown Skin
Product Code 18002550
- Little Junior Manikin in Brown Skin
- Soft Pack/Training Mat
- 2 Junior Faces
- 2 Junior Airways
- 6 Manikin Wipes
- Directions for Use
Reflective in size of a child, the Little Jr Brown Skin training manikin will allow students to practice their paediatric CPR skills as if they were in a real-life emergency.
The Little Jr Brown Skin provides trainers with a cost-effective option towards teaching paediatric CPR.
Ensuring your learners are aware of the differences between CPR and paediatric CPR will enable them to respond to almost any cardiac emergency, with confidence. Being the size of a child, the Little Jr Brown will ensure your learners are completely aware of the treatment required by a paediatric patient.
- Oral and nasal passages to allow for mouth-to-mouth and nose pinch practice
- Head tilt and jaw thrust maouever
About the Manufacturer
Laerdal's beginnings were in a small publishing house that specialised in children's books and greetings cards. Soon after they began to develop children's toys and eventually, first aid manikins.
Laerdal are now one of the world's leading developers and manufacturers of medical technology. They dedicate their time to developing products ranging in CPR training, AEDs, patient simulation and airway management.
If you would like to learn more about the Little Jr Brown Skin or any other product listed on our website, the defibshop team are always here to help.
To speak to one of our advisors, call 888 820 0760 and one of our team members will be happy to assist 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.