Modem door assembly

Modem door assembly

Product Code 11150-000009

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In Stock

What's Included?

  • Modem door assembly

Designed for use with the Lifepak 12 AED/ Monitor range from Physio Control, the Modem Door Assembly will allow you to install an Internal Modem into the device, further allowing you to transmit essential data. 

Without this assembly, the sharing of data on a Cellular or Land basis would not be possible as the modem could not be installed.

Being able to capture and share data captured by your AED will enable the emergency services to determine the potential cause of the cardiac arrest as well as determine the best possible aftercare for the patient.

About Physio Control

Physio Control was started up in 1955 by Dr Karl William Edmark and thirteen years later launched their very first AED/ Monitor to the world, the Lifepak 33.

Over time, their Lifepak range has developed with current technologies and has led them on to develop the Lifepak CR Plus, one of the world’s simplest yet recognizable AEDs.

Their vision of no one person dying due to a treatable, acute cardiac event is what motivates Physio Control to continue developing AEDs and saving lives. 

More Information

If you require more information about the Modem Door Assembly or Physio Control’s Lifepak AED range, the defibshop team are here to help.

To get in contact with one of our advisors, simply call 888 820 0760 and they’ll be happy to assist you to the best of their ability. 

 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.