Stryker · Model Visum 600
Stryker’s Visum 600 is a key component in the iSuite operating room that provides optimal light to the surgical site while accommodating all its users. Ideal attributes include: • Shadow resolution • Color rendering index • Maneuverability • Automatic reserve bulb • Heat dissipation
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: Pad alarm, no activation.
Root cause: Poor contact or expired pad.
Symptoms: Unintended or no activation.
Root cause: Fluid ingress / worn switch.
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.
Consumable per procedure.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Foot switch assembly | Periodic replacement | $$ | Fairly easy |
| OR light LED module | Major service part | $$$ | Difficult |
| Table hydraulic actuator | Periodic replacement | $$$ | Difficult |
| Electrosurgical pencil & electrode Consumable per procedure. | Consumable | $ | Easy |
Relative cost: $ lowest · $$$$ 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.
Synced live from the FDA openFDA API.
Offset Bushings associated with the lots identified were mismarked: the rotational reference numbers on the Tibial Offset Bushing were marked counterclockwise instead of clockwise; the Femoral Offset Bushing did not include rotational markings.
Unexpected powering down/failure to boot up: A problem with a transistor in the heater/temperature sensor component in the device may cause the device to power off during surgery or to fail to boot up at all. The risk includes delay and interruption of ongoing surgical procedures.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →