CooperSurgical · Model Leep System 6000
• Cut, Coag and Blend settings • Cut: 0-100 watts RMS • Blend 0-100 watts RMS • Coag 0-100 watts RMS • Footswitch operated
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: Poor cut/coag, sparking, low power.
Root cause: Burned/eroded blade or pencil.
Symptoms: Fractured tip, loose component, debris.
Root cause: Metal fatigue, improper reprocessing, or misuse.
Symptoms: Residue, bioburden, discoloration.
Root cause: Inadequate cleaning cycle or damaged tray.
Symptoms: Slow or drifting positioning.
Root cause: Cylinder seal or actuator wear.
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.
High-turnover consumable instruments.
Consumable per procedure.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| OR light LED module | Major service part | $$$ | Difficult |
| Table hydraulic actuator | Periodic replacement | $$$ | Difficult |
| Instrument repair / replacement set High-turnover consumable instruments. | Periodic replacement | $$ | Fairly easy |
| Electrosurgical pencil & electrode Consumable per procedure. | Consumable | $ | Easy |
Relative cost: $ lowest · $$$$ 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.
Synced live from the FDA openFDA API.
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.
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.
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator rather than the appropriate 3.15A slow blow fuses.
Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine HCl (2%) but contains vials Lidocaine HCl (1%)
Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of P/N R1010- Medium Radius Loop Electrode
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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