Chattanooga · Model Triton 4739
• 270° Pivoting User Interface • Digital High Resolution Color Touch Screen Interface • Patient Data Cards record up to 14 treatments, including patient pain mapping, pain scales and pain types • Store up to 80 user defined protocols for Cervical, Lumbar, Hip and Wrist traction • Clinical Resources Library with full color anatomical and pathological libraries • Quick-Link Indications to quickly retrieve preset treatment parameters • Detailed color treatment setup photos • Clinical Protocols™, complete with treatment rationale for Cervical, Lumbar, Hip and • Wrist traction • Softer, more comfortable traction pulls • Progressive and Regressive Steps with Independent timer • Traction in Static, Intermittent or Cycling with independent timer • Pre-tension Mode • Variable Speed Motor
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: Unresponsive controls, won't power on.
Root cause: PSU or control board aging.
Symptoms: Loose joints, unstable frame.
Root cause: Fastener/bearing wear from repeated use.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Power supply unit | Major service part | $$ | Moderate |
| Control panel / PCB | Major service part | $$$ | 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.
Synced live from the FDA openFDA API.
Product contains an improper bracket for the transducer.
Product contains an improper bracket for the transducer.
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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