FIFIAB SPA · Model F6749RUSA
ECG patient cables 10 leads with defibrillator protection, Resistance 10 kOhm, with 4mm plug.
Intended use: A switching device to which electrocardiograph (ECG) limb and chest leads may be attached. It is used to connect various combinations of limb and chest leads to the output terminals in order to create standard lead combinations (e.g., leads I, II and III). This device will typically be used when the devices to be connected are from different manufacturer's, enabling them to mate together. This is a reusable device.
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Symptoms: Short charge-hold, low-battery on readiness test.
Root cause: Aged battery pack.
Symptoms: No shock delivered, pad error.
Root cause: Worn paddles or expired pads.
Symptoms: Won't charge or discharges unexpectedly.
Root cause: Relay/contactor wear.
Symptoms: Leakage alarm, self-test fail.
Root cause: Failed isolation components.
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Critical, keep charged spares.
Expiration-dated consumable.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Patient interface cable | Periodic replacement | $$ | Fairly easy |
| Rechargeable battery pack Critical, keep charged spares. | Periodic replacement | $$$ | Fairly easy |
| HV energy storage capacitor | Major service part | $$$$ | Expert-level |
| Defibrillation electrodes / pads Expiration-dated consumable. | Consumable | $$ | 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 structured starting point derived from the failure modes above. 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.
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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