Physio Control LIFEPAK 1000 with ECG Display
Physio Control LIFEPAK 1000 with ECG Display
Product Code 99425-000025
- Physio-Control LIFEPAK 1000 AED
- 3 Sets of ECG Electrodes
- Lithium Battery
- Soft Carry Case
- Rescue Kit
- 3-Wire Cable
- Shoulder Strap
- Quick Reference Manual
- 5 Year Manufacturer's Warranty
- FREE defibcare Essential AED Program License for 1 Year
The LIFEPAK 1000 AED is a robust and hard-wearing device, fully equipped with LCD screen to provide ECG data as well as real-time graphics and colour instructions.
The perfect all-rounder, the LIFEPAK 1000’s helpful step-by-step visual and vocal prompts will allow users of limited training to provide an effective rescue and will appeal to the more professional rescuer with its built-in ECG capability.
- Dual display options make the Lifepak 1000 adaptable to your patient's needs
- Clear visual and voice prompts help the first responder through the rescue process, so even untrained users can provide lifesaving support
- Simple, intuitive user interface
- Pre-connected electrodes help to speed up the rescue process during the vital minutes after someone has suffered a sudden cardiac arrest
- High-capacity battery provides the power for up to 440 shocks, approximately 17 hours of monitoring time
- Digital recorded ECG rhythm and delivered shocks can be wirelessly transferred to a PC for review
LIFEPAK 1000 Features
ADAPTIV biphasic technology
The LIFEPAK 1000’s built-in ADAPTIV software allows the AED to deliver escalating shocks (200 - 360 joules) based on previous treatment delivered and the patient’s reaction to defibrillation, helping to provide the most effective treatment.
The LIFEPAK 1000 was NASA’s AED of choice to first be sent into space in 2008.
Want to learn more about the LIFEPAK 1000 AED device? Our helpful team of AED specialists are waiting to take your call. To get in touch, simply call 800 989 7768.
5 Year Manufacturer's Warranty
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.