Mettler Toldeo · Model Mettler SysStim 206A
One-channel neuromuscular stimulator The Sys*Stim 206 is a one-channel neuromuscular stimulator that features four different waveforms in a light-weight package. The narrow pulse is suited for TENS while the wide and AC pulses can be used for muscle stimulation. Direct Current can be used to stimulate denervated muscles or perform iontophoresis. The Sys*Stim 206 is an ideal companion to the Sonicator 716 for combination therapy.
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 stimulation, skin irritation.
Root cause: Adhesive/surface wear.
Symptoms: Intermittent stimulation, no output on one channel.
Root cause: Repeated flexing at connector.
Symptoms: Output won't adjust, stuck at one level.
Root cause: Potentiometer or control board 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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Rechargeable battery | Periodic replacement | $ | Fairly easy |
| TENS / stim electrodes Consumable. | Consumable | $ | Easy |
| Lead wire set | Frequent wear item | $ | 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.
The recall was initiated because Mettler has confirmed the possible failure of internal mechanical component and software detection for potential failure regarding Electronics Traction Device - MTD4000. The firm are initiating the recall because component failure might result in patient injury. Use of the device should cease immediately.
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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