Rotaid Solid Plus Heat Red Cabinet

Rotaid-Solid-Plus-Heat

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Rotaid Solid Plus Heat Red Cabinet

Product Code 11996-000451

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What's Included?

    The Rotaid Cabinet Family

  • Rotaid Solid Plus Heat Cabinet in Red
  • Alarm System
  • Automated Heating System
  • LED Lighting

Designed for outdoor use in temperatures of -5°F and above and complete with an automated heating system and LED lights, the Rotaid Solid Plus Heat cabinet provides protection from dust and water.

For AED storage in a variety of outdoor environments, the Rotaid Solid Plus with Heating the built in heating system will measure and control the temperature in the cabinet. With an IP55 rating, this cabinet will protect your AED from dust and water jets.

Key Features

Pre-drilled mounting holes on top of the backplate with mounting hardware included

Protection against dust and water

Solid Steel Hook on the bottom for a seal, instructions, or label

4 Mounting Positions for secure attachment

Cover with directional arrows for guidance

6 Indents for optimal grip to quickly open

Specifications

Size

Dimensions:W48cm x H48cm x D18cm

Weight: 14.77lbs

Electronic Features

Alarm System

Power Supply: 2 AAA Batteries

Output: 90dB

Operating/Storage Temperature

For outdoor use, designed for temperatures of -5°F / -20°C and above.

More Information

If you have any questions about the Rotaid Solid Plus Heat Cabinet, give us a call at 800 989 7768 and a team member will assist 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.