Excel HSE pack in Sofia Metal wall cabinet

Excel HSE pack in Sofia Metal wall cabinet

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Excel HSE pack in Sofia Metal wall cabinet

Product Code 171

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What's Included?

  • Excel HSE pack in Sofia Metal wall cabinet

The perfect storage solution to house all of your medical supplies, this Sofia Metal Wall Cabinet allows you to store your spare products effectively so you can always refill your first aid kit. (Contents not included).

Keeping your first aid kit stocked up is essential for ensuring the safety of your employees and colleagues. Your kit should contain all the vital equipment needed for assisting a casualty with a first aid injury at all times and so keeping spares is extremely helpful to ensure you’re never caught without.  

Benefits of Use

We always urge you to keep spare first aid materials to hand at all times, to ensure your first aid kit is never without the core equipment in a first aid emergency.

By keeping your supplies in a designated cabinet, you can keep on top of your first aid maintenance in keeping a good supply of materials on site to replenish your kit with.  In addition to this, employees will always know where they can replace an item if it has been used to ensure a full compliant kit at all times.

More Information

Want to learn more about this product? Our clued-up team of defibshop advisors are on hand to help.

You can get in touch by calling 0845 071 0830 where a member of our team will be happy to assist you with any queries you may have, to find the perfect product for you. 

 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.

In 2014 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 2017, 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 27001. 

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.