
Defibtech · Model Lifeline AUTO
Simple, One-Button Operation Clear Voice Prompts Long Life Battery Designed for the Real-World Active Status Indicator Highly Visible Award-Winning Ergonomic Design Rugged and Durable Easy to Upgrade Easy to Record and Transfer Data Safe and Effective Life Saving Technology Corporate Focus and Commitment.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Delivered energy outside tolerance on the analyser, will not charge, or charges slowly.
Root cause: HV capacitor / charging-circuit ageing, or an output-relay fault.
Symptoms: Short standby, readiness indicator shows service, unit fails the self-test on battery.
Root cause: Aged battery pack or a charging fault.
Symptoms: "Check pads", "connect electrodes", no ECG through pads, poor paceing capture.
Root cause: Worn therapy cable, expired pads, or a paddle / connector fault.
Symptoms: A monitoring parameter drops or is implausible.
Root cause: Patient cable / sensor or the parameter module.
Symptoms: No printout, event data will not transfer.
Root cause: Thermal recorder or the data / Wi-Fi interface.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Battery pack | Periodic replacement | $$ | Easy |
| Therapy / defib cable | Periodic replacement | $$ | Fairly easy |
| Multifunction pads | Frequent wear item | $ | Easy |
| HV / charging board | Major service part | $$$$ | Difficult |
| Thermal recorder / print head | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Within the Irish Market, a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life. There is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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