Laerdal Premature Anne Task Trainer
Laerdal Premature Anne Task Trainer
Product Code 290-00050
- SimMom Birthing lubricant
- Laerdal Airway Lubricant 45ml
- Simulated Blood Concentrate
- Umbilical cords (3)
- 42mm Face Mask
- 3M “Kind Removal Silicone Tape”
- 10ml Syringe
- Hat and Blanket
- User guide and Important Product Information
- Tray for the storage of the Task Trainer
Developed in conjunction with the American Academy of Pediatrics (AAP), the Premature Anne Task Trainer is a realistically proportioned 25-week preterm manikin that allows trainers to train healthcare professionals in the initiation of correct care and resuscitation of pre-term infants.
The Premature Anne Task Trainer is packaged in a box that has been designed for both training and storage use with the simulated headboard on the rear end of the package.
- Realistically proportioned
- Can be used in a variety of clinical settings
About the Manufacturer
Since their start in 1940, Laerdal have moved on from being a small publishing house that specialized in greetings cards and children's books to one of the world's leading medical equipment manufacturers.
Their training manikins are the first choice for many medical professionals and they have helped educate over 400 million people in life-skills.
If you would like to learn more about the Premature Anne Task Trainer, the defibshop team are here to help.
Simply call 800 989 7768 to speak to one of our advisors and they'll be happy to answer any questions or queries you may have.
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.