ZEISS · Model EyeMag Light II
Two powerful rechargeable battery packs Charging cradle Offers coaxial light, resulting in minimal shadow formation Clearly defined illuminated field
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: Unintended or no activation.
Root cause: Fluid ingress / worn switch.
Symptoms: Slow or drifting positioning.
Root cause: Cylinder seal or actuator wear.
Symptoms: Dim or dead panel, color shift.
Root cause: LED module aging.
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.
Consumable per procedure.
Single-use; expiry critical.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Electrosurgical pencil & electrode Consumable per procedure. | Consumable | $ | Easy |
| Return electrode (patient plate) Single-use; expiry critical. | Consumable | $ | Easy |
| Foot switch assembly | Periodic replacement | $$ | Fairly easy |
| OR light LED module | Major service part | $$$ | Difficult |
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.
The manufacturer confirmed that the opto-semiconductor sensors can be triggered by exposure to incandescent lighting. The safety interlock is in place to prevent unintended exposure to Class 3B laser radiation.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →