CooperSurgical LEEP System 1000
CooperSurgical · Model LEEP System 1000
Power output and LED display for ease of access/use. Flush faceplate membrane facilitates operation and cleaning. Microprocessor-controlled for increased precision, accuracy, reproducibility, and safety. Provides a choice of Cut, Blend, and Coag waveforms to accommodate subtle differences in technique and electrode performance. Pneumatic foot pedal for maximum safety. Audible safety features include distinct tones for each operating setting. Automatic self-test mechanism ensures accurate system operation.
Key tips
- ·Never defeat or bypass a return-electrode monitoring (REM) alarm to finish a case - it's a direct burn risk.
- ·Verify OR table battery backup - a table that loses power mid-procedure is a real, documented incident type.
- ·Track surgical light lamp-hours rather than waiting for failure - a sudden failure mid-case is avoidable.
Typical Failure Modes
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.
No or low RF output / high impedance cut-out
HighSymptoms: 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.
Return-electrode (patient-plate) contact-quality alarm
MediumSymptoms: 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.
Bipolar / vessel-sealing output fault
MediumSymptoms: Bipolar or sealing output weak, seal cycle will not complete, instrument not recognised.
Root cause: Bipolar cable / instrument fault or the sealing output stage.
Fails calibration after a repair / output drifts
MediumSymptoms: Output power or the REM circuit outside tolerance on the analyser, calibration will not pass.
Root cause: Output board or REM circuit needs recalibration (required after component replacement) - anti-static handling required.
Footswitch / handswitch fault
MediumSymptoms: Output will not activate from the pedal or the handpiece.
Root cause: Footswitch or handswitch / cable fault.
Touchscreen / display / boot fault
LowSymptoms: Unresponsive touchscreen, will not power on or boot, fan / thermal alarm.
Root cause: Display, power supply, control board, or a cooling-fan fault.
Serviceable Parts & Consumables
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.
Reusable instrument / handpiece cables
Class Periodic replacementRel. cost $$R&R Easy
Split dispersive (return) pads
Class ConsumableRel. cost $R&R Easy
Footswitch
Class Periodic replacementRel. cost $$R&R Fairly easy
Bipolar / sealing cable
Class Periodic replacementRel. cost $$R&R Easy
RF output board
Recalibration required after replacement; anti-static handling.
Class Major service partRel. cost $$$$R&R Difficult
Cooling fan
Class Major service partRel. cost $R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Reusable instrument / handpiece cables | Periodic replacement | $$ | 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.
PM Checklist
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.
- ·Pre-case functional check
- ·Electrosurgical return-electrode cable inspection
- ·Table hydraulic / mechanical inspection
- ·Annual electrical safety test and full PM
Troubleshooting Approach
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.
Symptom: No / low RF output or high impedance
- Confirm good electrode-tissue contact and an adequately wetted field.
- Inspect the handpiece / instrument and cable for damage; substitute known-good.
- Check the split dispersive pad is well applied with full skin contact and a good cable.
- Verify output into a resistive test load with an electrosurgical analyser.
- Replace the output board and recalibrate if output is confirmed absent (anti-static workplace; Erbe/OEM-trained personnel only for ERBE units).
Symptom: Return-electrode / plate alarm
- Re-apply a fresh split dispersive pad with full skin contact over well-perfused muscle.
- Check the pad cable and connector.
- Try a known-good pad.
- Run the contact-quality-monitor calibration if it still alarms with a good pad.
- Do calibration on a non-conductive surface.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Operating rooms
- Procedure rooms
- Interventional suites
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.
- RECALL
Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.
- RECALL
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
- RECALL
2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator rather than the appropriate 3.15A slow blow fuses.
- RECALL
Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine HCl (2%) but contains vials Lidocaine HCl (1%)
- RECALL
Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of P/N R1010- Medium Radius Loop Electrode
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