Masimo SET Red Pediatric Reusable Direct Connect Sensor - 3 foot

Masimo SET Red Pediatric Reusable Direct Connect Sensor - 3 foot

Imagenes Adicionales

Masimo SET Red Pediatric Reusable Direct Connect Sensor - 3 foot

Product Code 11996-000333

0 reviews

En existencia

What's Included?

  • Masimo SET Red Pediatric Reusable Direct Connect Sensor - 3 foot

The 3 foot Masimo SET Red Pediatric Reusable Direct Connect Sensor by Physio-Control is for use with the LIFEPAK 15 AED and is ideal for spot checking and short term monitoring paediatric casualties. 

Equipped with Masimo SET pulse oximeter technology, Masimo SET provides the most accurate and reliable SpO2 and pulse rate measurements including under the most challenging clinical conditions. The sensor is comfortable for the casualty and easy to clean for re-use.

About the Manufacturer

Physio Control is a world leader in the development, manufacture, sale, and service of AEDs and other emergency medical response products and services. Their Lifepak range is one of the most popular in the world, being the preferred choice for many Emergency Medical Services, as well as schools and public locations. Their AEDs provide a wide range of defibrillators which are tailored to suit everyone’s level of expertise.

 

More Information

If you would like to find out more about the Masimo SET Red Pediatric Reusable Direct Connect Sensor, do not hesitate to get in touch and a member of the defibshop team will be more than happy to help with any questions or queries you may have. Why not give them a call on 888 820 0760.

 

 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.