Heartstart OnSite First Aid Training Unit
Heartstart OnSite First Aid Training Unit
Product Code M5085A-ABA
- Carry Case
- 1 Adult Training Pads Cartridge
- 1 External Manikin Adaptor
- Quick Reference Guide
- Directions for Use
The Philips Heartstart OnSite First Aid Training Unit will help potential users understand how the Philips OnSite AED will operate during a real-life cardiac emergency.
Unique and simplistic in design, the HrtStrt Trainer by Laerdal has been developed to educate learners on how to effectively use HeartStart Onsite and HeartStart Home clinical AED range.
To ensure your trainees are receiving the correct training, this device is compliant with the 2010 Guidelines.
- Eight preconfigured scenarios
- Audible CPR coaching
- Capable of providing step by step instructions for performing CPR, including compression-to-ventillation ratios and the length of each ventillation
- Voice instructions match those of the clinical HeartStart OnSite and HeartStart Home AEDs
About the Manufacturers
Laerdal's training manikins have helped educate over 400 million people in essential life-skills and are the choice of healthcare professionals around the world.
Did you know, the company started off in a small publishing house that specialized in children's books and greetings cards?
If you require more information about the Philips HrtStrt Trainer, speak to the team here at defibshop.
Get in touch by calling 888 820 0760 and one of our advisors will be happy to share their knowledge with 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.