Stryker · Model TPS
Total Performance Arthroscopy Shaver Console Works with the Stryker 12K Shaver Handpiece.
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: Weak or stalled blade rotation.
Root cause: Motor brush wear or drive coupling fatigue.
Symptoms: Console won't power on, or resets mid-case.
Root cause: Main board or power supply failure.
Symptoms: No response, or intermittent activation.
Root cause: Worn footswitch pedal or connector.
Symptoms: Arcing, or no RF output.
Root cause: Worn electrode connector contacts.
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.
Major R&R; sterilizable handpiece wears fastest.
High-turnover; keep spares.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Footswitch / pedal assembly | Periodic replacement | $$ | Fairly easy |
| Console main board | Major service part | $$$ | Difficult |
| Handpiece motor assembly Major R&R; sterilizable handpiece wears fastest. | Periodic replacement | $$$$ | Difficult |
| Blade / burr coupling High-turnover; keep spares. | Periodic replacement | $$ | Fairly 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.
It was discovered that the silicone potting failed to properly cure after undergoing the prescribed curing possess. The potting material is used to insulate, stabilize and provide a moisture barrier to the TPS MicroDriver main Printed Circuit Board Assembly (PCBA). Inadequate cure of the silicone potting could potentially allow it to leak to the outside of the handpiece or cause an electrical ma
The safety margin values detailed in the Engineering Design were entered incorrectly into the programming software. Handpieces that have been programmed with the incorrect parameters could result in unintended activation. There is a potential for injury to the patient or user as a result of unintended forward or reverse activation. There is also the potential that the handpiece may not reach 100
There is a potential for these blades to break where the blade is welded on to the arbor. This hazard can result in the following harms: tissue damage due to the broken blade being aspirated or swallowed, additional surgery to remove a broken blade, infection due to an unretrieved device component, complications associated with increased time under anesthesia to retrieve a broken blade, osteomyeli
Product was packaged with an incorrect packaging material and therefore has a potential to be non-sterile which, if contaminated, could lead to a patient infection.
Lack of assurance of sterility.
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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