
Nipro Diagnostics · Model TRUEresult
7- 14- and 30-day averaging. 4 testing reminder alarms. Audible fill detection. Weekday display. Glucose control detection. Hematocrit range – 20-60%. Ketone test reminder. Alternate site testing. Strip release button. Automatic on/off.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Result flagged or biased, QC control out of range, strip / cartridge error code.
Root cause: Expired or mishandled strips / cartridges, a temperature / hematocrit interference, or an optics / electrode fault.
Symptoms: Strip not detected, error on insertion, intermittent contact.
Root cause: Contaminated or worn strip-port contacts / optics.
Symptoms: Dead unit, short battery life, will not charge.
Root cause: Depleted or aged battery.
Symptoms: Operator / lot barcode will not scan, results not sent to the docking / LIS.
Root cause: Barcode reader or the docking-station / wireless link.
Symptoms: Missing segments, unresponsive buttons.
Root cause: Display or keypad fault.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Test strips / cartridges | Frequent wear item | $$ | Easy |
| QC control solutions | Frequent wear item | $ | Easy |
| Battery | Frequent wear item | $ | Easy |
| Strip-port contacts / optics module | Periodic replacement | $$ | Moderate |
| Docking station / barcode reader | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Manufactured with an incorrect factory set unit of measure.
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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