Product Code 96576
- Carry Case
The robust HeartSave Carry Case is built to protect your defibrillator in harsh environments. The case includes a built-in pressure release valve that prevents water and dust from entering and potentially damaging the machine. The case is also waterproof, with sealing neoprene and can even withstand shocks from the defibrillator.
The HeartSave carry case is available in a range of colours. The standard options are black and orange, but other options are available upon request.
How to Use
Store your defibrillator in this hard wearing case to protect it when you’re on the move. This case would be ideal for first responders travelling to the site of an emergency, or for an outdoor environment like a construction site where the defibrillator may be exposed to dust or water.
You can also store essential items that will help make your role a little easier. The case provides extra space for pads, batteries and other accessories like gloves, a razor, face shield and scissors. Storing these items alongside the defibrillator will improve the efficiency of the rescue process, giving the patient an increased chance of survival.
About the Manufacturer
Primedic is an innovative medical technology production company based in Germany who distribute products all over the world. Primedic combine expertise with cutting edge technology to produce innovative lifesaving products.
Do you need further information about the HeartSave Carry Case? Please do not hesitate to ask. Our experienced defibshop team are more than happy to help with any enquiries that you may have. Contact defibshop today on 0845 071 0830.
Want to know why you should choose us? Press play and find out more...
And if it couldn't get any better..
- We have over 50 different defibrillators available and we can help you decide the best one for you
- We have over 200 trainers nationwide to deliver nationally accredited training in the use of a defib and CPR
- Over 20 staff on hand to offer impartial advice on all things defibrillators
- 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
Did we also mention we are an Award Winning company?
We’re sure that you have been past our Home Page, but in case you haven’t, skipping the intro and getting stuck into the world of defibrillators, we are an award winning company.
This year we added an impressive trophy to the cabinet by being listed 22nd in the ‘Great Place to Work: Best Workplaces 2014’ Small Business Category.
We also have to our name Salford Business Excellence Award Runner Up 2014 & 2012, Investors in People – Bronze Award and an Insight 100 Customer Service Award in Training Services 2013 award.
We also have a number of accreditations under our belt, including being a TQUK Diamond Approved Centre, ISO 9001 and 14001 and CIEH.
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.