Aivia 220 AED Cabinet Seal Protected with Audible Alarm

Aivia 220 AED Cabinet Seal Protected with Audible Alarm

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Aivia 220 AED Cabinet Seal Protected with Audible Alarm

Product Code 2A220-100ie

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What's Included?

    • Aivia 220 AED Cabinet Seal Protected with Audible Alarm

 

The Aivia 220 cabinet can be installed either indoors or outdoors to give your defibrillator a safe storage place depending on your needs, and with seal protection, your defibrillator is comprehensively protected from the weather if stored outside whilst the alarm feature alerts the public that there is a medical emergency occuring.

With the ability to install this cabinet both in indoor and outdoor environments, you can ensure your device is visible and accessible to bystanders in the event of a cardiac emergency.

Unique Features

  • Cabinet is suitable for both indoor and outdoor environments
  • Built with two compartments to provide it with shock resistance properties
  • Combines polycarbonate cover with ABS chassis
  • Visual aid shown on front of cabinet to show key stages of rescue progress
  • LEDs installed within cabinet for day/night lighting
  • Equipped with internal heating
  • 105db audible alarm triggered when cabinet is opened

Benefits

With no access code required, this cabinet is a great option for most locations to allow potential rescuers to retrieve an AED quickly in an emergency situation.

Once the cabinet is opened, the audible alarm will trigger alerting people in the nearby area that an emergency rescue is taking place. This provides the first responders with additional assistance and so they can focus wholly on getting life-saving treatment to the victim as soon as possible.

 Want to know why you should choose us? Press play and find out more...

Buying a defibrillator? You’ve come to the right place...

  • With nearly 20 different defibrillator models available, our defibshop team knows them all and can help you decide which device suits your budget, environment and business
  • We have over 20 staff on hand who can offer friendly and impartial advice on all things defibrillators
  • Not only do we provide a free battery and electrode pad reminder service, but we will replace your electrode pads for free if they are used within two years of purchase

Did you know that we're an Award Winning company?

We’re not a company for bragging but we like to think that our trophy cabinet indicates that you have come to a trustworthy and dependable company who recognises you are making a significant and fantastic step when buying a defibrillator.

We were recently listed in the Small Business category of the 'Great Place to Work: Best Workplaces 2014’ whilst we have also won accolades in the Salford Business Awards 2014 & 2012, Investors in People Bronze award and an Insight 100 Customer Service Award in Training Services 2013.

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.