Physio-Control - LifePak 500 AED
DESCRIPTION
Defibrillator
The biphasic Medtronic Physio Control Lifepak 500 AED is designed to be used by first responders for cardiac arrest emergencies. The Lifepak 500 automated external defibrillator wieghs only 7 lbs and is very compact. Simple 2 or 3-button operation takes a responder through the defibrillation process with audio and visual prompts. Voice commands and display messages help guide through the defibrillation process. Automated daily self-tests and long-lasting batteries help ensure that only minimal maintenance is required. It is designed for safety and dependabilit. All Biphasic models come upgraded with the latest AHA guidelines. The Medtronic Physio Control Lifepak 500 is for adult use only: Not compatible with Pediatric Pads. There is a seperate Pediatric Lifepak 500 AED which is Pediatric compatible.
FORUMSView All (2)
4Replies7 years ago | To Reset AED lifepack 500 I need to know the RESET procedure to get rid of the "service wrench" indicator on the units.After testing with Defib analyzer the indicator remains on,do you need special software to flash the unit ?Can anyone help with this.Thankyou.Reply |
2Replies8 years ago | battery and wrench error message the battery and wrench icons are showing, but when the battery is taken out and put back in, and then the machine is turned on, the OK icon shows. The lithium battery does not expire for another 10 months. What could be the issue? Reply |
DOCUMENTS / MANUALSView All
SERVICE COMPANIESView All Defibrillator Companies
FEATURES
- Always visible readiness display
- Simple 2- or 3-button operation
- Low maintenance
- Portable, lightweight
- Rugged, durable
- Powerful, user-friendly data management
- Compatible with Medtronic
- Physio-Control electrodes and
- LIFENET® data management system
Height | 10.2 cm |
Weight | 6.2 lbs |
Defibrillator Type | External, Automated (AED) |
Width | 26.7 cm |
FDA AlertsView All
Class 1 Recall: Physio-Control Inc. Recalls Defibrillation...
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.