AIVIA 200 Cabinet with Fan

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AIVIA 200 Cabinet with Fan

Product Code U2A200UXX100

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What's Included?

  • Cabinet
  • Power Supply

The AIVIA 200 Cabinet is suitable for storing your AED in an indoor and outdoor environment, to keep your device safe and secure. The contents of this cabinet will not be mistaken as the clear signage states the contents of the cabinet is a life-saving AED.

This AIVIA 200 cabinet includes a fan and an audible and visual alarm used for public access which is powered by the 24VDC Power Supply provided. 

Please note: The power supply must be hard-wired into the facility's electrical system.  

The signage on this cabinet ensures the AED is not mistaken, allowing it to be located and retrieved at ease in an emergency. The chain of survival is printed on the front to provide assistance to a rescue.

Key Features

  • A luminosity sensor automatically activates flashing white LEDs to help identify the location of the AIVIA 200 in low light situations
  • Open access to the AED is protected by security seals 
  • Removing the AED automatically triggers a visually red flashing LED alarm as well as an audible alarm to alert bystanders of an incident
  • The visual alarm will also signal anomalies such as an out of range temperature

Dimensions -  Length: 15 1/4" Height: 16 5/8" Depth: 7 15/16"

More Information

Got a question about the AIVIA 200 cabinet with Fan or any of our other products? Do not hesitate to get in touch with a member of the defibshop team by calling 800 989 7768.

 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.