
Boston Scientific · Model Endostat III
A self-limiting energy system that is designed to limit the depth of burn penetration. A variable speed peristaltic pump intended to provide precisely controlled irrigation. Two bipolar modes: CONTINUOUS or VARIABLE TIME, designed to vary the duration of energy delivery. The monopolar capabilities of the Endostat III Generator are intended to provide physicians the ability to perform certain therapeutic procedures using standard monopolar devices such as polypectomy snares, sphincterotomes, and hot biopsy forceps. A choice of four individual RF waveforms: COAG, BLEND, CONTROL CUT, or CUT. Receptacles that accept widely used monopolar active cords and disposable dispersive electrodes (patient plates, or grounding pads). The Endostat III Generator also features a new safety standard that utilizes two separate warning systems intended to help identify the cause of a problem and prevent surgical error. The “Pad Fault” warning system is designed to detect a poor connection between the generator and the pad or between the pad and the patient. In the event of a fault, the RF power is designed to be inhibited until the connection is corrected. The unit is also designed to monitor the output and the internal power supplies. If the output or internal supplies exceed their specified limits, the unit is designed to go into a “System Fault” condition, which is intended to prohibit any output. Also, the unit is designed with a maximum single power application time limit of 22 seconds, as a safety feature in case of a footswitch activation failure.
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: No cut / coag effect, "high impedance" or output-error message, output shuts down.
Root cause: Poor electrode contact or a dry field, a damaged handpiece / cable, a return-electrode (REM/NESSY) fault, or an output-stage fault.
Symptoms: REM / NESSY / plate alarm, monopolar output inhibited.
Root cause: Poorly applied or dried split dispersive pad, a pad-cable fault, or the contact-quality-monitor circuit.
Symptoms: Bipolar or sealing output weak, seal cycle will not complete, instrument not recognised.
Root cause: Bipolar cable / instrument fault or the sealing output stage.
Symptoms: Output power or the REM circuit outside tolerance on the analyser.
Root cause: Output board or REM circuit needs recalibration - anti-static handling required.
Symptoms: Output will not activate from the pedal or the handpiece.
Root cause: Footswitch or handswitch / cable fault.
Symptoms: Unresponsive touchscreen, will not power on or boot, fan / thermal alarm.
Root cause: Display, power supply, control board, or a cooling-fan fault.
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.
Recalibration required after replacement; anti-static handling.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Reusable instrument / handpiece cables | Periodic replacement | $$ | Easy |
| Split dispersive (return) pads | Consumable | $ | Easy |
| Footswitch | Periodic replacement | $$ | Fairly easy |
| Bipolar / sealing cable | Periodic replacement | $$ | Easy |
| RF output board Recalibration required after replacement; anti-static handling. | Major service part | $$$$ | Difficult |
| Cooling fan | Major service part | $ | Moderate |
Relative cost: $ lowest · $$$$ 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.
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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