Laerdal Resusci Jr with SkillGuide
Laerdal Resusci Jr with SkillGuide
Product Code 18001101
- Full Body Pediatric Manikin
- Hard Carry Case
- Training Mat
- Skillguide™ Unit
- Track Suit
- 4 Junior Faces
- 4 Junior Airways
- 12 Manikin Wipes
- Directions for Use
The Resusci Jr training manikin has been designed to specifically teach child resuscitation and rescue techniques. This Resusci Jr is accompanied by the optional SkillGuide CPR performance indicator.
Designed specifically to teach about the rescue and resuscitation techniques that should be used on a child, the Resusci Jr will ensure your trainees feel confident in emergencies to deliver effective CPR to a child.
The SkillGuide included with the Resusci Jr is a CPR performance indicator that provides immediate feedback on ventilation duration and volume, compression depth and hand position to further enhance your trainee's knowledge.
- Realistic features
- Anatomically correct
- Head tilt and jaw thrust manouever
- Chest rise verifies correct ventilations
- Realistic resistance for chest compressions
About the Manufacturer
Laerdal are one of the world's leading first aid equipment manufacturers, developing technologies that range in CPR training, airway management, AEDs and patient simulation.
Their beginnings are quite different to other first aid manufacturers. Did you know they started off as a small publishing house in 1940?
If you require more information about the Resusci Jr with SkillGuide, the defibshop team are here to help.
Simply call 800 989 7768 to speak to one of our specialists and they'll be happy to help 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.